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741721-49-3

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741721-49-3 Usage

General Description

2,5-difluoro-3-nitrobenzoic acid is a chemical compound with the molecular formula C7H3F2NO4. It is a derivative of benzoic acid with two fluorine atoms and a nitro group attached to the benzene ring. 2,5-difluoro-3-nitrobenzoic acid is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic materials. It is also a potential candidate for use in the development of new drugs due to its unique chemical properties. Additionally, 2,5-difluoro-3-nitrobenzoic acid has been studied for its potential applications in materials science and as a precursor in organic synthesis. Its versatile nature and reactive functional groups make it a valuable compound for various research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 741721-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,7,2 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 741721-49:
(8*7)+(7*4)+(6*1)+(5*7)+(4*2)+(3*1)+(2*4)+(1*9)=153
153 % 10 = 3
So 741721-49-3 is a valid CAS Registry Number.

741721-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Difluoro-3-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,2,5-difluoro-3-nitro

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:741721-49-3 SDS

741721-49-3Upstream product

741721-49-3Relevant articles and documents

RAF INHIBITOR COMPOUNDS AND METHODS OF USE THEREOF

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Page/Page column 40, (2011/04/14)

Compounds of Formula (I) are useful for inhibition of Raf kinases. Methods of using compounds of Formula (I) and stereoisomers, tautomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment

N- (6-AMINOPYRIDIN-3-YL) -3- (SULFONAMIDO) BENZAMIDE DERIVATIVES AS B-RAF INHIBITORS FOR THE TREATMENT OF CANCER

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Page/Page column 48, (2009/10/22)

Compounds of Formula (I) are useful for inhibition of Raf kinases. Methods of using compounds of Formula I and stereoisomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed.

Synthesis and structure-activity studies of novel benzocycloheptanone oxazolidinone antibacterial agents

Vara Prasad,Boyer, Frederick E.,Chupak, Lou,Dermyer, Michael,Ding, Qizhu,Gavardinas,Hagen, Susan E.,Huband, Michael D.,Jiao, Wenhua,Kaneko, Takushi,Maiti, Samarendra N.,Melnick, Michael,Romero, Karina,Patterson,Wu, Xiujuan

, p. 5392 - 5397 (2007/10/03)

We describe a novel class of benzocycloheptanone derived oxazolidinone antibacterial agents. The synthesis and antibacterial activities with structure variation is discussed.

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