Category: 111865-47-5

Chen, Fener published the artcileSynthesis of ibuprofen by rearrangement, Recommanded Product: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, the publication is Zhongguo Yiyao Gongye Zazhi (1992), 23(1), 1-2, database is CAplus.

On the basis of the Giordano’s method, ibuprofen was synthesized with some improvements in 75% overall yield from isobutylbenzene. The mild reaction conditions, convenient work-up and higher purity of the product were advantages of this method.

Zhongguo Yiyao Gongye Zazhi published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, Recommanded Product: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Guo, Libing published the artcileSynthesis of N-(4-biphenyl)-(9,9-dimethyl-2-fluorenyl)amine, Category: bromides-buliding-blocks, the publication is Huaxue Tongbao (2010), 73(8), 750-752, database is CAplus.

2-Bromofluorene was prepared from fluorene and benzyltrimethylammonium tribromide in dichloromethane-methanol solution at room temperature, followed by a reaction with iodomethane in THF in the presence of potassium tert-butanolate and formation of 9,9-dimethyl-2-bromo-9H-fluorene. The synthesis of the target compound was achieved by a Buchwald-Hartwig reaction of the above-mentioned aryl bromide with [1,1′-biphenyl]-4-amine and the product thus obtained was confirmed by ¹H-NMR, ¹³C-NMR, MS, IR spectra and elemental anal.

Huaxue Tongbao published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, Category: bromides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Wu, Liqiang published the artcileSynthesis of 6-bromoquinolines using benzyltrimethylammonium tribromide, Category: bromides-buliding-blocks, the publication is Youji Huaxue (2010), 30(8), 1250-1254, database is CAplus.

Several 6-bromoquinoline derivatives were designed and the synthesis of the target compounds was achieved in high yield by a reaction of 2-aminobenzophenone [i.e., (2-aminophenyl)(phenyl)methanone] with α-methylene carbonyl compounds in the presence of benzyltrimethylammonium tribromide as a phase-transfer catalyst in acetonitrile at room temperature and the products thus obtained were confirmed by ¹H-NMR, ¹³C-NMR spectra and elemental anal. The title compounds thus reported included 8-bromo-10-phenyl-11H-indeno[1,2-b]quinolin-11-one, 2-bromo-12-phenylbenz[b]acridine-6,11-dione and 6-bromo-4-phenylquinoline derivatives, 7-bromo-9-phenyl-1H-cyclopenta[b]quinoline derivatives, etc.

Youji Huaxue published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C5H8N2O, Category: bromides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Liu, Fan published the artcileHole Transport Materials Based on 6,12-Dihydroindeno[1,2-b]fluorine with Different Periphery Groups: A New Strategy for Dopant-Free Perovskite Solar Cells, Quality Control of 111865-47-5, the publication is Advanced Functional Materials (2019), 29(24), n/a, database is CAplus.

Although several hole-transporting materials (HTMs) have been designed to obtain perovskite solar cells (PSCs) devices with high performance, the dopant-free HTMs for efficient and stable PSCs remain rare. Herein, a rigid planar 6,12-dihydroindeno[1,2-b]fluorine (IDF) core with different numbers of bulky periphery groups to construct dopant-free HTMs of IDF-SFXPh, IDF-DiDPA, and IDF-TeDPA is modified. Thanks to the contributions of the planar IDF core and the twisted SFX periphery groups, the dopant-free IDF-SFXPh-based PSCs device achieves a device performance of 17.6%, comparable to the doped 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (spiro-OMeTAD)-based device (17.6%), with much enhanced device stability under glovebox and ambient conditions.

Advanced Functional Materials published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, Quality Control of 111865-47-5.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Smith, J. Anthony published the artcileAcridones and Quinacridones: Novel Fluorophores for Fluorescence Lifetime Studies, Safety of Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, the publication is Journal of Fluorescence (2004), 14(2), 151-171, database is CAplus and MEDLINE.

Two new families of fluorescent probe, acridones and quinacridones, whose fluorescence lifetime can be altered to produce a range of lifetimes from 3 ns to 25 ns are described. Both families of fluorophore have fluorescence lifetimes which are unaffected by pH in the range of 5 to 9 and show a marked resistance to photobleaching. The probes have been modified to allow them to be attached to biomols. and the labeling of a neuropeptide (substance P) is described. The labeled peptides have the same fluorescence lifetime as the free fluorophore. Quinacridone, with an emission around 550 nm offers a long fluorescence lifetime, photostable alternative to fluorescein.

Journal of Fluorescence published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C6H12N2O, Safety of Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Goel, Shruti published the artcileKinetics and mechanism of the oxidation of organic sulfides by benzyltrimethylammonium tribromide, Name: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, the publication is Journal of Chemical Research, Synopses (1996), 510-511, database is CAplus.

The oxidation of organic sulfides by benzyltrimethylammonium tribromide involves formation of a halo sulfonium cation in the slow step and its subsequent decomposition in the fast step to give sulfoxides.

Journal of Chemical Research, Synopses published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, Name: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Ito, Akihiro published the artcileA spiro-fused triarylaminium radical cation with a triplet ground state. [Erratum to document cited in CA139:036205], Application In Synthesis of 111865-47-5, the publication is Angewandte Chemie, International Edition (2009), 48(32), 5785, database is CAplus.

On page 923, Equation 2 is incorrect; the correct version of the equation is given. In this article, in the right-hand column on page 923, the optimized value for the exchange coupling J should be corrected to J=11.2cm^-1 (=16.0 K), and Reference [3] cited in this paragraph should be Reference [6].

Angewandte Chemie, International Edition published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, Application In Synthesis of 111865-47-5.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Okamoto, Tsuyoshi published the artcileOxidation using quaternary ammonium polyhalides. V. Selective oxidation of benzyl alcohols by the use of benzyltrimethylammonium tribromide, Quality Control of 111865-47-5, the publication is Bulletin of the Chemical Society of Japan (1989), 62(11), 3748-9, database is CAplus.

The reaction of several substituted benzyl alcs. with 1 equiv of PhCH₂N⁺Me₂ Br^– in carbon tetrachloride under basic or neutral conditions gave the corresponding benzaldehydes. With 2 equiv of PhCH₂N⁺Me₃ Br^– in aqueous alk. solution and subsequent acid hydrolysis, the corresponding benzoic acids were obtained in satisfactory yields.

Bulletin of the Chemical Society of Japan published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, Quality Control of 111865-47-5.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Arai, Ryota published the artcileReversible photoinduced change in molecular ordering of diarylethene derivatives at a solution-HOPG interface, SDS of cas: 111865-47-5, the publication is Journal of the American Chemical Society (2008), 130(29), 9371-9379, database is CAplus and MEDLINE.

A diarylethene-pyrene diad and a diarylethene-pyrene-diarylethene triad were synthesized to investigate the photoinduced two-dimensional ordering change at a solution-HOPG interface. The mol. arrangements were detected by STM. The different photochromic isomers showed different orderings reflecting the differences in their mol. structures. For the diarylethene-pyrene-diarylethene triad, a new ordering appeared upon irradiation with UV light and returned to the original ordering upon subsequent irradiation with visible light. The new arrangement was assigned to the ordering of the closed-closed isomers based on the images of the isolated open- and closed-isomers. The relationship between the nature of the two-dimensional ordering and the mol. structure is discussed.

Journal of the American Chemical Society published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, SDS of cas: 111865-47-5.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Vetter, Walter published the artcileIdentification and quantification of new polybrominated di-methoxybiphenyls (PBDMBS) in marine mammals from Australia, Recommanded Product: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, the publication is Organohalogen Compounds (2008), 2388-2391, database is CAplus.

This study aims to verify the hypothesis by the photolytical debromination as well as synthesis of dibromo and tribromo congeners related to 2,2′-diMeO-BB 80, followed by the screening of these products in environmental samples. Using the authentic standard of 2,2′-diMeO-BB 80, it was for the first time possible to quantify residues of 2,2′-diMeO-BB 80 in blubber of dolphins and cetaceans from Australia. Moreover, the calibrated solution of lower BDMBs offered the opportunity to determine these debromination products of 2,2′-diMeO-BB 80 as well. The concentrations of the 2,2′-diMeO-BB 80 related BDMBs were 0.43-1.5% of 2,2′-diMeO-BB 80.

Organohalogen Compounds published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H10O6, Recommanded Product: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary