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1-bromo-4-(octylthio)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76542-23-9

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76542-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76542-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,4 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76542-23:
(7*7)+(6*6)+(5*5)+(4*4)+(3*2)+(2*2)+(1*3)=139
139 % 10 = 9
So 76542-23-9 is a valid CAS Registry Number.

76542-23-9Relevant academic research and scientific papers

A general, efficient, and functional-group-tolerant catalyst system for the palladium-catalyzed thioetherification of aryl bromides and iodides

Fernandez-Rodriguez, Manuel A.,Hartwig, John F.

body text, p. 1664 - 1672 (2009/07/17)

The cross-coupling reaction of aryl bromides and iodides with aliphatic and aromatic thiols catalyzed by palladium complexes of the bisphosphine ligand CyPF-tBu (1) is reported. Reactions occur in excellent yields, broad scope, high tolerance of functional groups, and with turnover numbers that exceed those of previous catalysts by 2 or 3 orders of magnitude. These couplings of bromo- and iodoarenes are more efficient than the corresponding reactions of chloroarenes and could be conducted with less catalyst loading and/or milder reaction conditions. Consequently, limitations regarding scope and functional group tolerance previously reported in the coupling of aryl chlorides are now overcome.

CuI-catalyzed coupling reactions of aryl iodides and bromides with thiols promoted by amino acid ligands

Deng, Wei,Zou, Yan,Wang, Ye-Feng,Liu, Lei,Guo, Qing-Xiang

, p. 1254 - 1258 (2007/10/03)

Novel mild conditions for the CuI-catalyzed coupling reactions of aryl iodides and bromides with aliphatic and aromatic thiols using amino acids as the ligand are reported.

A new class of second-order non-linear optical material: Stilbazolium benzimidazolate derived from alkylsulfonyl substituted stilbazole

Nemoto, Nobukatsu,Abe, Jiro,Miyata, Fusae,Shirai, Yasuo,Nagase, Yu

, p. 1193 - 1197 (2007/10/03)

A novel stilbazolium benzimidazolate derivative, i.e. 2-(4-{2-[4-(octylsulfonyl)phenyl]ethenyl}pyridinio)benzimidazolate 4a, was prepared by the quaternization reaction of 4-{2-[4-(octylsulfonyl)phenyl]ethenyl}pyridine with 2-chlorobenzimidazole, followed by deprotonation with aqueous ammonia. Poly(methyl methacrylate) (PMMA) thin films containing 10 or 20 mass% of 4a were obtained by spin-coating from their THF solutions on an ordinary cover glass substrate. Second-harmonic generation (SHG) measurements of the obtained thin films were carried out by the Maker fringe method using a Q-switched Nd : YAG laser (1064 nm) as an exciting beam after corona-poling. A poled PMMA film containing 10 or 20 mass% of 4a exhibited a second-order non-linear optical (NLO) coefficient, d33, of 7.6 or 11 pm V-1, respectively, which was much larger than the d33 value of a PMMA thin film containing 10 mass% of 2-[4-(2-phenylethenyl)pyridinio]benzimidazolate 4c (d33 1.6 pm V-1) or 2-{4-[2-(4-octyloxyphenyl)ethenyl]pyridinio}benzimidazolate 4d (d33 0.51 pm V-1). There were no significant differences in linear absorption properties of PMMA films containing 4a, 4c or 4d. The introduction of an octylsulfonyl group at the 4′-position of the stilbazole moiety increases the second-order NLO coefficient.

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