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1,4-Cyclohexadiene-1,2-dicarboxylic acid, 3-methyl-5-(trimethylsilyl)-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106212-32-2

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106212-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106212-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,2,1 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106212-32:
(8*1)+(7*0)+(6*6)+(5*2)+(4*1)+(3*2)+(2*3)+(1*2)=72
72 % 10 = 2
So 106212-32-2 is a valid CAS Registry Number.

106212-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dicarbomethoxy-3-methyl-5-(trimethylsilyl)cyclohexa-1,4-diene

1.2 Other means of identification

Product number -
Other names 3-Methyl-5-trimethylsilanyl-cyclohexa-1,4-diene-1,2-dicarboxylic acid dimethyl ester

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:106212-32-2 SDS

106212-32-2Downstream Products

106212-32-2Relevant academic research and scientific papers

Regioselective Alkylation of 3-(Trimethylsilyl)-3-sulfolene: Route to Stereospecific 2-Silylated Butadiene Derivatives

Tao, Yu-Tai,Chen, Man-Li

, p. 69 - 72 (2007/10/02)

Dichotomous regiochemistry in the alkylation of 3-(trimethylsilyl)-3-sulfolene (1) can be achieved by controlling the amount of base used (to generate the monoanion or the dianion) and the sequence of its addition.In this way, a variety of 2-silyl-1,3-but

Convenient Syntheses of Silylated 1,3-Dienes

Chou, Ta-shue,Tso, Hsi-Hwa,Tao, Yu-Tai,Lin, Lung Ching

, p. 244 - 246 (2007/10/02)

Several 2- or 3-silylated 3-sulfolenes have been prepared from 3-sulfolenes by the direct deprotonation/substitution sequence.These sulfolenes serve as the stable precursors for the silylated 1,3-dienes and can be used directly in Diels-Alder reactions without isolation of the diene intermediates.

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