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3-bromo-5-trimethysilyltoluene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

315668-55-4

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315668-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315668-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,6,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 315668-55:
(8*3)+(7*1)+(6*5)+(5*6)+(4*6)+(3*8)+(2*5)+(1*5)=154
154 % 10 = 4
So 315668-55-4 is a valid CAS Registry Number.

315668-55-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-5-trimethysilyltoluene

1.2 Other means of identification

Product number -
Other names 5-methyl-3-trimethylsilyl-1-bromobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:315668-55-4 SDS

315668-55-4Relevant academic research and scientific papers

Synthesis of shape-persistent macrocycles by a one-pot suzuki-miyaura cross-coupling reaction

Huang, Weiguo,Wang, Ming,Du, Chun,Chen, Yulan,Qin, Ruiping,Su, Linjie,Zhang, Chi,Liu, Zhengping,Li, Cuihong,Bo, Zhishan

supporting information; experimental part, p. 440 - 444 (2011/03/18)

Ring creation: Shape-persistent macrocyclic structures were prepared by a one-pot catalyst-transfer Suzuki-Miyaura cross-coupling (CTSMCC) reaction (see figure). The reaction of 3,6-dibromo-substituted carbazoles and diboronic ester monomers afforded shap

An easy and multigram-scale synthesis of versatile AA- and AB-type w-terphenylenes as building blocks for kinked polyphenylenes

Kissel, Patrick,Breitier, Simon,Reinmueller, Viktoria,Lanz, Patrick,Federer, Lukas,Schlueter, A. Dieter,Sakamoto, Junji

supporting information; experimental part, p. 2953 - 2955 (2009/11/30)

A set of m-terphenylenes having a readily functionalizable hydroxy group as well as either symmetric AA-type or unsymmetric AB-type halide termini have been prepared on a several-gram scale. The synthesis was carried out on the basis of the Suzuki-Miyaura

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