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80437-08-7

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80437-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80437-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80437-08:
(7*8)+(6*0)+(5*4)+(4*3)+(3*7)+(2*0)+(1*8)=117
117 % 10 = 7
So 80437-08-7 is a valid CAS Registry Number.

80437-08-7SDS

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 benzyl 2-trifluoroacetoxy-1-octyl sulfide

1.2 Other means of identification

Product number -
Other names 1-benzylthio-2-trifluoroacetoxyoctane

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:80437-08-7 SDS

80437-08-7Relevant articles and documents

Additions to Alkenes via Metal Ion-Promoted Oxidation of Dialkyl and Diaryl Disulphides

Bewick, Alan,Mellor, John M.,Owton, W. Martin

, p. 1039 - 1044 (2007/10/02)

Reactions of alkenes with di-n-propyl, diphenyl, and dibenzyl disulphide in the presence of lead(IV) salts in trifluoroacetic acid-dichloromethane are described.The products, vicinal trifluoroacetoxysulphides, are obtained in higher yields with manganese(III) salts as the oxidant.Alternative reaction conditions with use of iron(III) salts or in the absence of added metal salts are also described.Trifluoroacetoxysulphides derived from diphenyl disulphide react with acetonitrile under Ritter conditions to give acetamidosulphides but trifluoroacetoxysulphides derived from dibenzyl disulphide only give the vicinal acetamidosulphides in poor yield as a result of an alternative reaction pathway affording benzylacetamide.Conversions of acetamidosulphides into aminosulphides and into acetamidothiols are described.

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