Category: 80480-15-5

Efficient synthetic method for the preparation of allyl- and propargyl-epoxides by allylation and propargylation of α-haloketones with organozinc reagents was written by Pan, Jie;Zhang, Min;Zhang, Songlin. And the article was included in Organic & Biomolecular Chemistry in 2012.Safety of 2-Bromo-1-(pyren-1-yl)ethanone The following contents are mentioned in the article:

A simple, efficient, and non-metal catalyzed synthetic method for the preparation of substituted allyl- and propargylepoxides by allylation and propargylation of α-halo ketones with organozinc reagents in mild conditions is reported in this paper. The present method complements the existing synthetic methods due to some advantageous properties of the organozinc reagents such as availability, selectivity, operational simplicity and low toxicity. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Safety of 2-Bromo-1-(pyren-1-yl)ethanone).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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. 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 2-Bromo-1-(pyren-1-yl)ethanone

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

New class of 8-aryl-7-deazaguanine cell permeable fluorescent probes was written by Dhimitruka, Ilirian;Eubank, Timothy D.;Gross, Amy C.;Khramtsov, Valery V.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2015.Reference of 80480-15-5 The following contents are mentioned in the article:

A one step synthesis of fluorescent 8-aryl-(7-deazaguanines) has been accomplished. Probes exhibit blue to green high quantum yield fluorescence in a variety of organic and aqueous solutions, high extinction coefficients, and large Stokes shifts often >100 nm. The probes are highly cell permeable, and exhibit stable bright fluorescence once intracellular; therefore are suited to the design of biosensors. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Reference of 80480-15-5).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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. 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.Reference of 80480-15-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Acetylpyrene-labelled 7-methylguanine nucleotides: unusual fluorescence properties and application to decapping scavenger activity monitoring was written by Kasprzyk, Renata;Kowalska, Joanna;Wieczorek, Zbigniew;Szabelski, Mariusz;Stolarski, Ryszard;Jemielity, Jacek. And the article was included in Organic & Biomolecular Chemistry in 2016.Product Details of 80480-15-5 The following contents are mentioned in the article:

7-Methylguanosine (m⁷G) nucleotides labeled with acetylpyrene (AcPy) were synthesized as fluorescent mRNA 5′ end (cap) analogs. The unique fluorescent properties of m⁷G-AcPy conjugates, different from G-AcPy, can be applied to studying various mRNA cap-related processes including the evaluation of putative inhibitors of DcpS enzyme, a therapeutic target in neuromuscular diseases. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Product Details of 80480-15-5).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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). 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.Product Details of 80480-15-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Research advances on monensin-II and development of analysis method was written by Wei, Rui-cheng;Wang, Ran;Liu, Tie-zheng. And the article was included in Zhongguo Shouyi Xuebao in 2007.Application In Synthesis of 2-Bromo-1-(pyren-1-yl)ethanone The following contents are mentioned in the article:

A review. Monensin is widely used in production, and is effective to Eimeria mitis in chicken, and effective to prevent coccidiosis for livestock, such as lamb, sheep, calf, rabbit. This paper involves development of methods to do a general description about monensin-II and its characteristics and the detection limit are analyzed and compared, for trying to continue to provide in-depth study. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Application In Synthesis of 2-Bromo-1-(pyren-1-yl)ethanone).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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. 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.Application In Synthesis of 2-Bromo-1-(pyren-1-yl)ethanone

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Synthesis of allyl-aziridines from α-halo oxime ethers and allyl zinc bromides was written by Zheng, Songlin;Zhang, Songlin. And the article was included in RSC Advances in 2016.Category: bromides-buliding-blocks The following contents are mentioned in the article:

A novel method for the preparation of substituted allyl aziridines by reaction of α-halo oxime ethers with allylic zinc reagents in mild conditions was reported. The present method complemented the existing synthetic methods due to some advantages offered by the use of organozinc reagents, which are easily prepared, relatively stable and non-toxic and more selective than Grignard reagents. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Category: bromides-buliding-blocks).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Visible Light Activation of Spin-Silenced Fluorescence was written by Eing, Matthias;Tuten, Bryan T.;Blinco, James P.;Barner-Kowollik, Christopher. And the article was included in Chemistry – A European Journal in 2018.Category: bromides-buliding-blocks The following contents are mentioned in the article:

A self-reporting, profluorescent, visible light-induced release system is introduced. Fluorescence activation is enabled by a mild remote trigger signal that can be monitored with the naked-eye in real time. The light-responsive spin-silenced polymer is synthesized via an Ugi post-polymerization modification incorporating paramagnetic nitroxides and a light cleavable fluorophore moiety. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Category: bromides-buliding-blocks).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. 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.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Pyreneacyl sulfides as a visible light-induced versatile ligation platform was written by Tuten, Bryan T.;Menzel, Jan P.;Pahnke, Kai;Blinco, James P.;Barner-Kowollik, Christopher. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2017.COA of Formula: C18H11BrO The following contents are mentioned in the article:

We report a visible light responsive moiety capable of generating highly reactive thioaldehydes. Upon irradiation with visible light (420 nm) the pyreneacyl sulfide species undergoes a Norrish II elimination yielding thioaldehydes capable of being trapped by nucleophiles (amines, aminoxys, and thiols), as well as Diels-Alder processes, representing a new versatile ligation platform. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5COA of Formula: C18H11BrO).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. 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.COA of Formula: C18H11BrO

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A very convenient synthesis of cyclopenta[cd]pyrene was written by Spijker, Nynke M.;Van den Braken-Van Leersum, Anne M.;Lugtenburg, Johan;Cornelisse, Jan. And the article was included in Journal of Organic Chemistry in 1990.SDS of cas: 80480-15-5 The following contents are mentioned in the article:

Friedel-Crafts acylation of pyrene with BrCH₂COBr in CH₂Cl₂ in the presence AlBr₃ afforded 1-(bromoacetyl)pyrene, which cyclized to cyclopentapyrenone I on irradiation in CCl₄. I was converted to cyclopenta[cd]pyrene by Wolff-Kishner reduction, followed by oxidation with DDQ. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5SDS of cas: 80480-15-5).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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–bromine bond is electrophilic in nature. 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.SDS of cas: 80480-15-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Synthesis of end-cap precursor molecules for (6,6) armchair and (9,0) zig-zag single-walled carbon nanotubes was written by Mueller, Andreas;Amsharov, Konstantin Yu.;Jansen, Martin. And the article was included in Tetrahedron Letters in 2010.Name: 2-Bromo-1-(pyren-1-yl)ethanone The following contents are mentioned in the article:

The synthesis and purification of a C₆₀H₃₀ precursor mol. for the end-cap of a (6,6) armchair and of a C₅₄H₂₄ precursor mol. for a (9,0) zig-zag type single-walled nanotube are described. An approach to controlled growth of single-walled carbon nanotubes is suggested. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Name: 2-Bromo-1-(pyren-1-yl)ethanone).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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: 2-Bromo-1-(pyren-1-yl)ethanone

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Synthesis, characterization of difunctionalized calix[4]arene containing pyrene and crown ether groups was written by Zhang, Dehua;Lv, Jian-quan. And the article was included in Huaxue Shiji in 2006.Application In Synthesis of 2-Bromo-1-(pyren-1-yl)ethanone The following contents are mentioned in the article:

A novel calix[4]arene-crown ether, 26,28-bis(1-acetylpyrene)-5,11,17,23-tetra-butyl-calix[4]arene-crown-6 was synthesized and characterized. The structures were confirmed by IR, ¹HNMR and elementary anal. The results showed that the derivative backbone adopted the cone conformation. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5Application In Synthesis of 2-Bromo-1-(pyren-1-yl)ethanone).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) 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–bromine bond is electrophilic in nature. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.Application In Synthesis of 2-Bromo-1-(pyren-1-yl)ethanone

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary