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804476-64-0

Acetic acid, difluoro[(2-hydroxyethyl)thio]-, ethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

804476-64-0

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804476-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 804476-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,4,4,7 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 804476-64:
(8*8)+(7*0)+(6*4)+(5*4)+(4*7)+(3*6)+(2*6)+(1*4)=170
170 % 10 = 0
So 804476-64-0 is a valid CAS Registry Number.

804476-64-0SDS

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 ethyl difluoro-(2-hydroxyethylsulfanyl)acetate

1.2 Other means of identification

Product number -
Other names Difluoro-(2-hydroxy-ethylsulfanyl)-acetic acid ethyl 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:804476-64-0 SDS

804476-64-0Downstream Products

804476-64-0Relevant articles and documents

Synthesis of fluoroalkyl vinyl sulfoxides and their use in Diels-Alder reactions

Moise, Joelle,Goumont, Regis,Magnier, Emmanuel,Wakselman, Claude

, p. 2297 - 2302 (2004)

Condensation of various dienes with fluoroalkyl vinyl sulfoxides was studied. Four diastereoisomers were obtained in the case of cyclopentadiene and their structures were assigned by 2D NMR experiments. Diels-Alder cycloaddition occurred with cyclohexadiene, in comparison to phenyl vinyl sulfoxide, without thermal extrusion of fluoroalkylsulfenic acid. Condensation with anthracene led to a mixture of compounds 11 and 12.

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