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20372-63-8

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20372-63-8 Usage

Chemical Properties

Solid

General Description

4,5-Difluoro-2-nitrobenzoic acid can be obtained from the nitration of 4,5-difluorobenzoic acid or 3,4-difluorobenzoic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 20372-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,7 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20372-63:
(7*2)+(6*0)+(5*3)+(4*7)+(3*2)+(2*6)+(1*3)=78
78 % 10 = 8
So 20372-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H3F2NO4/c8-4-1-3(7(11)12)6(10(13)14)2-5(4)9/h1-2H,(H,11,12)

20372-63-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H28935)  4,5-Difluoro-2-nitrobenzoic acid, 97%   

  • 20372-63-8

  • 1g

  • 383.0CNY

  • Detail
  • Alfa Aesar

  • (H28935)  4,5-Difluoro-2-nitrobenzoic acid, 97%   

  • 20372-63-8

  • 5g

  • 1137.0CNY

  • Detail

20372-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Difluoro-2-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 4,5-Difluoro-2-nitro benzoic acid

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:20372-63-8 SDS

20372-63-8Relevant articles and documents

PLATELET ADP RECEPTOR INHIBITORS

-

Page/Page column 31-33, (2008/06/13)

Compounds are provided which are useful as platelet ADP receptor inhibitors, for treating thrombosis and for reducing the likelihood and/or severity of a secondary ischemic event in a patient.

Synthesis and antibacterial activity of 2-substituted 6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids

Jung, Jae-Chul,Baek, Shin,Park, Oee-Sook

, p. 664 - 676 (2007/10/03)

A series of 2-substituted 6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids was prepared and evaluated for antibacterial activity. The 6-fluoro-2-methyl-1-prenyl-1,4-dihydro-7-(3,5-dimethylpiperazinyl)-4-oxo-3-quinolinecarboxylic acid (14f) exhibited

Preparation of 2-choloro-4,5-difluorobenzoic acid from 4,5-difluorophthalic anhydride of 4,5-difluorophthalic acid

-

, (2008/06/13)

2-Chloro-4,5-difluorobenzoic acid may be prepared by decarboxylating 4,5-difluorophthalic anhydride or 4,5-difluorophthalic acid by heating in N-methyl-2-pyrrolidone or dimethyl acetamide optionally using copper, copper oxide, copper salts, or halides or salts of Zn, Cd, Ag and Ni as a catalyst to form 3,4-difluorobenzoic acid, reacting said 3,4-difluorobenzoic acid with a mixture of nitric and sulfuric acids to form 2-nitro-4,5-difluorobenzoic acid, reacting said 2-nitro-4,5-difluorobenzoic acid with elemental chlorine at a temperature of between 185° and 195° C. to form 2-chloro-4,5-difluorobenzoic acid.

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