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7304-32-7

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7304-32-7 Usage

Description

2-Fluoro-5-nitrobenzoic acid is an organic compound characterized by the presence of a fluorine atom at the 2nd position and a nitro group at the 5th position on a benzene ring, with a carboxylic acid functional group. It is a versatile building block in organic synthesis and has potential applications in the pharmaceutical and chemical industries.

Uses

Used in Pharmaceutical Synthesis:
2-Fluoro-5-nitrobenzoic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds, including dibenz[b,f]oxazepin-11(10H)-ones and substituted dibenzazocines. It is utilized in the nucleophilic aromatic substitution (SNAr) reaction with the hydroxyl (OH) group of various 2-aminophenols and immobilized polysubstituted phenols on solid support, enabling the formation of these complex heterocyclic structures.
Used in Chemical Synthesis:
2-Fluoro-5-nitrobenzoic acid is employed as a starting material in the synthesis of oxazepines, a class of heterocyclic compounds with potential applications in various chemical and pharmaceutical processes. Its reactivity and functional group compatibility make it a valuable component in the development of new chemical entities and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 7304-32-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7304-32:
(6*7)+(5*3)+(4*0)+(3*4)+(2*3)+(1*2)=77
77 % 10 = 7
So 7304-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H4FNO4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3H,(H,10,11)/p-1

7304-32-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B22100)  2-Fluoro-5-nitrobenzoic acid, 98%   

  • 7304-32-7

  • 1g

  • 238.0CNY

  • Detail
  • Alfa Aesar

  • (B22100)  2-Fluoro-5-nitrobenzoic acid, 98%   

  • 7304-32-7

  • 5g

  • 821.0CNY

  • Detail
  • Alfa Aesar

  • (B22100)  2-Fluoro-5-nitrobenzoic acid, 98%   

  • 7304-32-7

  • 25g

  • 3488.0CNY

  • Detail

7304-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-5-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-fluoro-5-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:7304-32-7 SDS

7304-32-7Relevant articles and documents

Discovery of novel 2-phenylamino-4-prolylpyrimidine derivatives as TRK/ALK dual inhibitors with promising antitumor effects

Cao, Zhi,Guo, Ming,Jiang, Nan,Li, Changtao,Li, Tong,Wang, Xinyu,Yang, Jing,Zhai, Xin

, (2021/10/06)

In order to explore novel TRK and ALK dual inhibitors, a series of 2-phenylamino-4-prolylpyrimidine derivatives were designed, synthesized and evaluated for their in vitro cytotoxicity and enzymatic activities. Delightfully, most compounds were detected m

New strategy for detection of hydrogen peroxide based on bi-nucleophilic reaction

Liu, Xiang,Mao, Chenxin,Tian, Yafei,Wang, Bei,Wang, Shuoshuo

supporting information, (2021/07/14)

Two novel fluorescent probes based on 7-hydroxy-4-methyl-coumarin, FAA-MC-OH (2-fluoro-4-nitro-phenylacetyl hydroxyl coumarin) and FBA-MC-OH (2-fluoro-4-nitro-benzoyl hydroxyl coumarin) are first synthesized, and spectral studies confirm that both the pro

2-HYDROXYISOQUINOLINE-1,3(2H,4H)-DIONES AND RELATED COMPOUNDS USEFUL AS HIV REPLICATION INHIBITORS

-

Page/Page column 83, (2012/07/13)

The present invention relates to compounds and compositions acting as inhibitors of HIV integrase. The compound of the invention is of Formula (I), or a tautomer (I') thereof, or a pharmaceutically acceptable salt, or solvate of said compound or tautomer

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