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Benzenepropanenitrile, b-(trimethylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34732-44-0

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34732-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34732-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,3 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34732-44:
(7*3)+(6*4)+(5*7)+(4*3)+(3*2)+(2*4)+(1*4)=110
110 % 10 = 0
So 34732-44-0 is a valid CAS Registry Number.

34732-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyano-2-phenyl-2-trimethylsilylethane

1.2 Other means of identification

Product number -
Other names -

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:34732-44-0 SDS

34732-44-0Relevant academic research and scientific papers

A new silicon-mediated elimination-rearrangement

Menichetti, Stefano,Stirling, Charles J. M.

, p. 1511 - 1515 (2007/10/03)

Treatment of trimethylsilylethanes bearing α-phenyl groups and β-phenylthio, phenylsulfonyl or cyano groups with LDA causes elimination-rearrangement mediated by the β-carbanionic species. Mechanistic conclusions are based on isotopic labelling experiment

Electroreductive silylation of activated olefins using a reactive metal anode

Ohno,Nakahiro,Sanemitsu,Hirashima,Nishiguchi

, p. 5515 - 5516 (2007/10/02)

Electroreductive silylation of α, β-unsaturated esters, nitriles and ketones in the presence of Me3SiCl using a reactive metal anode (Mg, Zn, Al) in an undivided cell afforded the corresponding β-silyl compounds offering a valuable method for introduction of a silyl group into activated olefins.

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