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431-71-0

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431-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 431-71-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 431-71:
(5*4)+(4*3)+(3*1)+(2*7)+(1*1)=50
50 % 10 = 0
So 431-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C3HF5O/c4-2(5)1(9)3(6,7)8/h2H

431-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,3,3-pentafluoropropan-2-one

1.2 Other means of identification

Product number -
Other names 1,1,1,3,3-pentafluoro-2-propanone

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:431-71-0 SDS

431-71-0Relevant articles and documents

-

Utebaev,U. et al.

, (1974)

-

Polyfluorinated enol acetates

Zeifman, Yu. V.,Postovoi, S. A.,German, L. S.

, p. 170 - 172 (1994)

The synthesis of polyfluorinated enol acetates has been performed by reductive dechlorination of chloropolyfluoroketones with zinc in Ac2O.Under these conditions, hexafluoroacetone is preferably reduced at the carbonyl group. - Key words: polychlorofluoroketones; reductive dehalogenation; polyfluorinated enol acetates; synthesis; reactivity.

METHOD OF MAKING HYDROFLUOROCARBONS

-

Page 18, (2008/06/13)

A method of producing hydrofluorocarbons and methods of producing other commercially attractive compounds formed as by-products of hydrofluorocarbon production by using aldehydes as a principal reactant.

REDUCTIVE DEFLUORINATION OF HEXAFLUOROACETONE ANIL

Zeifman, Yu. V.

, p. 186 - 188 (2007/10/02)

Hexafluoroacetone anil smoothly adds methyllithium at the C=N bond but undergoes reductive defluorination upon the action of Grignard reagents or metallic zinc to give 2-phenylaminopentafluoropropylene.

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