Category: 96761-85-2

Yamato, Takehiko et al. published their research in Journal of Chemical Research, Synopses in 1996 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.COA of Formula: C24H15Br3

Synthesis and crystal inclusion properties of 1,3,5-tris(para-substituted aryl)benzenes and double-decker phanes was written by Yamato, Takehiko;Hideshima, Chieko;Nagano, Yoshiaki;Tashiro, Masashi. And the article was included in Journal of Chemical Research, Synopses in 1996.COA of Formula: C24H15Br3 This article mentions the following:

A wide range of inclusion behavior is found for 1,3,5-tris(4-hydroxyphenyl)benzene 3 and 1,3,5-tris(4-alkoxyphenyl)benzenes on recrystallization from various solvents; a double-decker phane derived from 3 also forms a crystalline inclusion complex with toluene, but does not give any observable host-guest interaction in solution In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2COA of Formula: C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.COA of Formula: C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Golestanzadeh, Mohsen et al. published their research in ChemistrySelect in 2019 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Formula: C24H15Br3

Effect of Confined Spaces in the Catalytic Activity of 1D and 2D Heterogeneous Carbon-Based Catalysts for Synthesis of 1,3,5-Triarylbenzenes: RGO-SO3H vs. MWCNTs-SO3H was written by Golestanzadeh, Mohsen;Naeimi, Hossein. And the article was included in ChemistrySelect in 2019.Formula: C24H15Br3 This article mentions the following:

One hot debate between catalytic activities of sulfonated reduced graphene oxide (RGO-SO3H), as the 2D heterogeneous carbon-based catalyst, and sulfonated multi-walled carbon nanotubes (MWCNTs-SO3H), as the 1D heterogeneous carbon-based catalyst, was investigated in the synthesis of 1,3,5-triarylbenzenes under different conditions. This comparison study revealed that the 2D catalytic system was more efficient relative to the 1D catalyst in terms of yields of the target products, turnover frequency of the catalyst (TOF), and the reusability. The reasons of this observation such as sp. surface area, confinement spaces in 1D and 2D carbon-based catalysts, solvent accessible surface area, surface active sites, and the availability of supported functional groups on carbon nanostructures will discuss. Moreover, the application of synthesized compounds as a substrate was checked in carbon-carbon bond formation. Also, one of the synthesized compounds was produced using three approaches under metal and non-metal conditions. Notably, the recyclability of the two catalytic systems was checked. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Formula: C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Formula: C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Jang, Seokhoon et al. published their research in Synthetic Metals in 2018 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Pyrimidine based hole-blocking materials with high triplet energy and glass transition temperature for blue phosphorescent OLEDs was written by Jang, Seokhoon;Han, Si Hyun;Lee, Jun Yeob;Lee, Youngu. And the article was included in Synthetic Metals in 2018.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl This article mentions the following:

New hole-blocking materials (HBMs), mPyrPPB and pPPyrPB, consisting of pyrimidine and phenylene segments for high-performance blue phosphorescent OLEDs were designed and synthesized. The thermal, electrochem., and optical properties of mPyrPPB and pPPyrPB were systemically studied. The Tg values of mPyrPPB and pPPyrPB were 118 and 137闁? resp. The triplet energy and HOMO energy level of mPyrPPB were 2.77 eV and -6.86 eV, resp., indicating that it had sufficiently high triplet energy and deep HOMO energy level for the hole-blocking layer (HBL) in blue phosphorescent OLED devices. All the meta conjugation of mPyrPPB mol. structure effectively prevented 闁?electron delocalization and thus increased the triplet energy and electron transport property. MPyrPPB exhibited higher electron-transporting property than pPPyrPB because mPyrPPB possessed effective intermol. H bonds. When mPyrPPB was used as a HBM for a blue phosphorescent OLED device, external quantum efficiency (EQE), current efficiency (CE), and power efficiency (PE) values effectively increased to 16.4%, 36.7 cd/A, and 13.4 lm/W, resp. Compared to the reference device without HBM, EQE, CE, and PE increased by 38%, 35%, and 54%, resp., mainly due to the confinement of triplet excitons and holes and improved electron-transporting ability. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Su, Shi-Jian et al. published their research in Advanced Materials (Weinheim, Germany) in 2008 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.SDS of cas: 96761-85-2

Pyridine-containing triphenylbenzene derivatives with high electron mobility for highly efficient phosphorescent OLEDs was written by Su, Shi-Jian;Chiba, Takayuki;Takeda, Takashi;Kido, Junji. And the article was included in Advanced Materials (Weinheim, Germany) in 2008.SDS of cas: 96761-85-2 This article mentions the following:

Two pyridine-containing triphenylbenzene derivatives of 1,3,5-tri(m-pyrid-3-yl-phenyl)benzene (TmPyPB) and 1,3,5-tri(p-pyrid-3-yl-phenyl)benzene (TpPyPB) with high electron mobility and high triplet energy level are designed and synthesized. Highly efficient blue and green phosphorescent OLEDs are achieved by using TmPyPB and TpPyPB as an electron-transport layer, resp. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2SDS of cas: 96761-85-2).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.SDS of cas: 96761-85-2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wallon, Alexander et al. published their research in Chemische Berichte in 1990 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Many of the organo bromine compounds are relatively nonpolar. Bromine is more electronegative than carbon (2.8 vs 2.5) and hence the carbon in a carbon鑱砨romine bond is electrophilic in nature. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.Quality Control of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Pentamacrocyclic tris-crown hosts. Selective binding of cationic, anionic, and neutral guest compounds was written by Wallon, Alexander;Werner, Ute;Mueller, Walter M.;Nieger, Martin;Voegtle, Fritz. And the article was included in Chemische Berichte in 1990.Quality Control of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl This article mentions the following:

The tris-crown host compounds I [X, X1 = 1,3,5-C6H3 (Z), 1,3,5-(m-C6H4)3C6H3 (Z1), (p-C6H4)3CMe (Z2)] were synthesized for the first time. The x-ray crystal structures of I (X = Z, X1 = Z1) (II) the 1:3 complex of I (X = X1 = Z) (III) and KSCN were determined Whereas in the free crown II a less well preorganized mol. cavity is encountered, in the complex of III with KSCN one potassium ion is bound to each crown ether unit. One of the three SCN– anions is situated in the interior of the cavity and in addition is deoriented in such a way as to be bound to the K+ using partially the S atom of the SCN– ion. Organic guest mols. like 1,2-, 1,3-, 1,5-, 2,6-, and 2,7-naphthalenediol as well as 灏?naphthol in acidic water solution are bound selectively in the interior of the cavities of the host mol. II and I (X = X1 = Z1) but not by III and I (X = X1 = Z2) resp. In contrast, the binding of 浼?naphthol and of smaller phenolic guest mols. like phenol, resorcinol, pyrocatechol, phloroglucinol, pyrogallol, and 1,2,4-trihydroxybenzene with the hosts I is much less pronounced (1H-NMR highfield shifts). In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Quality Control of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Many of the organo bromine compounds are relatively nonpolar. Bromine is more electronegative than carbon (2.8 vs 2.5) and hence the carbon in a carbon鑱砨romine bond is electrophilic in nature. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.Quality Control of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wan, Jing et al. published their research in Journal of Materials Chemistry in 2012 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon閳ユ彽romine bond is electrophilic, i.e. alkyl bromides are alkylating agents. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Safety of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Multifunctional electron-transporting indolizine derivatives for highly efficient blue fluorescence, orange phosphorescence host and two-color based white OLEDs was written by Wan, Jing;Zheng, Cai-Jun;Fung, Man-Keung;Liu, Xiao-Ke;Lee, Chun-Sing;Zhang, Xiao-Hong. And the article was included in Journal of Materials Chemistry in 2012.Safety of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl This article mentions the following:

Derivatives of 1-azaindolizine are 1st used as electron-transporting host materials for hybrid fluorescence/phosphorescence white organic LEDs (F/P-WOLED). Of the azaindolizine derivatives, a blue fluorescent material BPPI (3-(4,4′-biphenyl)-2-diphenyl-1-azaindolizine) has: (1) blue emission with high quantum yields, (2) good morphol. and thermal stabilities, (3) electron-transporting properties, and (4) a sufficiently high triplet energy level to act as a host for red or yellow-orange phosphorescent dopants. The multifunctional BPPI enables adaptation of several simplified device configurations. For example, a nondoped blue fluorescent device exhibits good performance with an external quantum efficiency of 3.16% and Commission Internationale de l’Eclairage coordinates of (0.15, 0.07). A high-performance orange phosphorescent device has a high current efficiency of 23.9 cd A-1. Using BPPI, a F/P-WOLED with a simplified structure, stable emissions and respectable performance (current and external quantum efficiencies of 17.8 cd A-1 and 10.7%, resp.) was demonstrated. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Safety of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon閳ユ彽romine bond is electrophilic, i.e. alkyl bromides are alkylating agents. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Safety of 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yamato, Takehiko et al. published their research in Catalysis Letters in 1990 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.Synthetic Route of C24H15Br3

Solid superacids catalyzed organic synthesis. 3. Nafion-H catalyzed condensation of acetophenone derivatives. A preparative route to 1,3,5-triarylbenzenes. was written by Yamato, Takehiko;Hideshima, Chieko;Tashiro, Masashi;Prakash, G. K. Surya;Olah, George A.. And the article was included in Catalysis Letters in 1990.Synthetic Route of C24H15Br3 This article mentions the following:

Nafion-H, a perfluorinated resin sulfonic acid, catalyzes condensation of acetophenones I (R = H, R1 = H, alkyl, MeO, Br, Cl; R = Br, R1 = H) to provide 1,3,5-triarylbenzenes under relatively mild conditions. Reactions are clean and water formed as byproduct does not deactivate the catalyst. However, ortho-substituted acetophenones and 2-acetylthiophene gave no condensation product. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Synthetic Route of C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.Synthetic Route of C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Xiang, Zhihao et al. published their research in Materials Chemistry and Physics in 2020 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Theoretical study of a few 2D polymer networks and MOFs formed by chiral mTBPB molecules was written by Xiang, Zhihao;Kang, Shuangyu;Feng, Xuyang;Mu, Huijing;Cai, Yingxiang. And the article was included in Materials Chemistry and Physics in 2020.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl This article mentions the following:

Two-dimensional (2D) materials have become the most popular research targets due to their unique structural characteristics, novel phys. properties and potential applications such as photovoltaics, semiconductors, electrodes and water purification In this study, a few 2D polymer networks and their corresponding metal organic frameworks (MOFs) formed by the debromination (also including dehydrogenation) of mTBPB mols. were investigated based on first-principles calculations It was found that L-C48H30, LR-C48H30 and achiral-C12H6 were direct-bandgap semiconductors but L-C48H30Cr3, LR-C48H30Cr3 and achiral-C48H24Cr6 2D MOFs were ferromagnetic semiconductors. The origin of ferromagnetism in three 2D MOFs was mainly attributed to the contribution of Cr-d and C-pz orbitals. Furthermore, anisotropic carrier effective masses were determined and the reaction energy barriers to form these 2D polymer networks and MOFs were evaluated. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yamato, Takehiko et al. published their research in Journal of Chemical Research, Synopses in 1996 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.COA of Formula: C24H15Br3

Synthesis and crystal inclusion properties of 1,3,5-tris(para-substituted aryl)benzenes and double-decker phanes was written by Yamato, Takehiko;Hideshima, Chieko;Nagano, Yoshiaki;Tashiro, Masashi. And the article was included in Journal of Chemical Research, Synopses in 1996.COA of Formula: C24H15Br3 This article mentions the following:

A wide range of inclusion behavior is found for 1,3,5-tris(4-hydroxyphenyl)benzene 3 and 1,3,5-tris(4-alkoxyphenyl)benzenes on recrystallization from various solvents; a double-decker phane derived from 3 also forms a crystalline inclusion complex with toluene, but does not give any observable host-guest interaction in solution In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2COA of Formula: C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.COA of Formula: C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Golestanzadeh, Mohsen et al. published their research in ChemistrySelect in 2019 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Formula: C24H15Br3

Effect of Confined Spaces in the Catalytic Activity of 1D and 2D Heterogeneous Carbon-Based Catalysts for Synthesis of 1,3,5-Triarylbenzenes: RGO-SO3H vs. MWCNTs-SO3H was written by Golestanzadeh, Mohsen;Naeimi, Hossein. And the article was included in ChemistrySelect in 2019.Formula: C24H15Br3 This article mentions the following:

One hot debate between catalytic activities of sulfonated reduced graphene oxide (RGO-SO3H), as the 2D heterogeneous carbon-based catalyst, and sulfonated multi-walled carbon nanotubes (MWCNTs-SO3H), as the 1D heterogeneous carbon-based catalyst, was investigated in the synthesis of 1,3,5-triarylbenzenes under different conditions. This comparison study revealed that the 2D catalytic system was more efficient relative to the 1D catalyst in terms of yields of the target products, turnover frequency of the catalyst (TOF), and the reusability. The reasons of this observation such as sp. surface area, confinement spaces in 1D and 2D carbon-based catalysts, solvent accessible surface area, surface active sites, and the availability of supported functional groups on carbon nanostructures will discuss. Moreover, the application of synthesized compounds as a substrate was checked in carbon-carbon bond formation. Also, one of the synthesized compounds was produced using three approaches under metal and non-metal conditions. Notably, the recyclability of the two catalytic systems was checked. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Formula: C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Formula: C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary