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67640-39-5

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67640-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67640-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,4 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67640-39:
(7*6)+(6*7)+(5*6)+(4*4)+(3*0)+(2*3)+(1*9)=145
145 % 10 = 5
So 67640-39-5 is a valid CAS Registry Number.

67640-39-5SDS

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 2,4-difluorobenzoyl fluoride

1.2 Other means of identification

Product number -
Other names Benzoyl fluoride,2,4-difluoro

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:67640-39-5 SDS

67640-39-5Downstream Products

67640-39-5Relevant articles and documents

Halex reactions of aromatic compounds catalysed by 2-azaallenium, carbophosphazenium, aminophosphonium and diphosphazenium salts: A comparative study

Pleschke, Axel,Marhold,Schneider,Kolomeitsev,R?schenthaler

, p. 1031 - 1038 (2007/10/03)

An increasing number of biologically active compounds in the pharma and agro-chemical sector contain carbon fluorine bonds. One of the most common methods to introduce fluorine into intermediates is the well-investigated halogen-exchange reaction, in which chloro- and bromoaromatics activated towards nucleophilic substitution, react with a fluoride source to yield the corresponding fluoroarenes. In general, the reaction is supported by phase-transfer catalysts. The use of a new class of very active phase-transfer catalysts gives the possibility of substituting even halogens with weak activation giving a convenient access to interesting compounds that are not available so far and opening up new synthetic routes in Halex chemistry. Our new classes of catalysts, CNC+ (1a), PNC+ (2a) and several different approaches presented by other groups are described and experimental results discussed.

Process for the preparation of difluorobenzenes

-

, (2008/06/13)

Difluorobenzene is prepared by a multistep process involving fluorination of dichlorobenzoyl chloride to provide difluorobenzoyl fluoride, conversion thereof to difluorobenzoyl chloride, hydrogenation of this to difluorobenzaldehyde and decarbonylation of the aldehyde to difluorobenzene.

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