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Silane, trimethyl[(phenylthio)(2,4,6-trimethylphenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88534-31-0

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88534-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88534-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,3 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88534-31:
(7*8)+(6*8)+(5*5)+(4*3)+(3*4)+(2*3)+(1*1)=160
160 % 10 = 0
So 88534-31-0 is a valid CAS Registry Number.

88534-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[phenylsulfanyl-(2,4,6-trimethylphenyl)methyl]silane

1.2 Other means of identification

Product number -
Other names Silane,trimethyl[(phenylthio)(2,4,6-trimethylphenyl)methyl]

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:88534-31-0 SDS

88534-31-0Downstream Products

88534-31-0Relevant academic research and scientific papers

REACTION OF TRIMETHYLSILANE WITH ARENES AND ALK-1-ENES IN THE PRESENCE OF LEWIS ACID

Han, Dong Il,Oh, Dong Young

, p. 2213 - 2218 (2007/10/02)

trimethylsilane reacted with arenes and alk-1-enes in the presence of a Lewis acid to give the Friedel-Crafts product and the ene product, respectively.

Preparation of sulfines by alkylidenation of sulfur dioxide using α-silyl carbanions

Porskamp, P. A. T. W.,Leij, M. van der,Lammerink, B. H. M.,Zwanenburg, B.

, p. 400 - 404 (2007/10/02)

The synthesis of sulfines 4 from a series of active methylene compounds is described.Deprotonation, followed by silylation, gives the trimethylsilyl compounds 2.Subsequent deprotonation to α-silyl carbanions and treatment with an excess of sulfur dioxide

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