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105584-80-3

Silane, [(butylthio)phenylmethyl]triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105584-80-3

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105584-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105584-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,8 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105584-80:
(8*1)+(7*0)+(6*5)+(5*5)+(4*8)+(3*4)+(2*8)+(1*0)=123
123 % 10 = 3
So 105584-80-3 is a valid CAS Registry Number.

105584-80-3SDS

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 butyl α-triphenylsilylbenzyl sulphide

1.2 Other means of identification

Product number -
Other names (Butylsulfanyl-phenyl-methyl)-triphenyl-silane

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:105584-80-3 SDS

105584-80-3Downstream Products

105584-80-3Relevant articles and documents

Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides

Barbaro, Gaetano,Battaglia, Arturo,Giorgianni, Patrizia,Maccagnani, Gaetano,Macciantelli, Dante,et al.

, p. 381 - 386 (2007/10/02)

Trimethylsilyl and triphenylsilylaryl thioketones have been synthesized by acid catalysed reaction of the corresponding ketones with hydrogen sulphide.Such silylated thioketones heve been oxidized to give S-oxides and converted with diaryldiazomethanes into triaryl thiiranes; upon treatment with organolithium nucleophiles they undergo thiophilic addition.The ready desulphurization with triphenylphosphine of silylated thiirans to the corresponding silyl triaryl ethylenes is also reported.

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