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3-chloro-N-(4-fluorophenyl)benzamide is a chemical compound with the molecular formula C13H8ClFN2O. It is a benzamide derivative featuring a chlorine atom and a fluorophenyl group attached to the benzene ring. 3-chloro-N-(4-fluorophenyl)benzamide holds potential in pharmaceutical and medicinal chemistry due to the diverse biological activities associated with benzamides, such as antitumor and anti-inflammatory properties. The chloro and fluorophenyl groups present in the molecule may also contribute to its utility as a building block in the synthesis of more complex organic molecules. Further research and testing are required to fully explore its potential uses and properties.

33489-31-5

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33489-31-5 Usage

Uses

Used in Pharmaceutical Industry:
3-chloro-N-(4-fluorophenyl)benzamide is used as a potential antitumor agent for its possible role in inhibiting tumor growth and progression. Its benzamide structure and the presence of chloro and fluorophenyl groups may contribute to its effectiveness in this application.
Used in Medicinal Chemistry:
3-chloro-N-(4-fluorophenyl)benzamide is used as a potential anti-inflammatory agent, leveraging its benzamide properties to modulate inflammatory responses and alleviate symptoms associated with inflammation.
Used in Organic Synthesis:
3-chloro-N-(4-fluorophenyl)benzamide is used as a building block in the synthesis of other complex organic molecules, taking advantage of its unique structural features to create novel compounds with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 33489-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,8 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33489-31:
(7*3)+(6*3)+(5*4)+(4*8)+(3*9)+(2*3)+(1*1)=125
125 % 10 = 5
So 33489-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H9ClFNO/c14-10-3-1-2-9(8-10)13(17)16-12-6-4-11(15)5-7-12/h1-8H,(H,16,17)

33489-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-N-(4-fluorophenyl)benzamide

1.2 Other means of identification

Product number -
Other names 3-chlorophenyl-N-(4-fluorophenyl)benzamide

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:33489-31-5 SDS

33489-31-5Relevant academic research and scientific papers

Role of Hetero-halogen (F · · · X, X = Cl, Br, and I) or homo-halogen (X · · · X, X = F, Cl, Br, and I) interactions in substituted benzanilides

Nayak, Susanta K.,Kishore Reddy,Row, Tayur N. Guru,Chopra, Deepak

experimental part, p. 1578 - 1596 (2012/04/04)

A series of halogen-substituted benzanilides have been synthesized and characterized, and crystallization studies directed toward generation of polymorphs have been performed to delineate the importance of interactions involving halogens. The effect of ha

Synthesis and biological relationships of 3′,6-substituted 2-phenyl-4-quinolone-3-carboxylic acid derivatives as antimitotic agents

Lai, Ya-Yun,Huang, Li-Jiau,Lee, Kuo-Hsiung,Xiao, Zhiyan,Bastow, Kenneth F.,Yamori, Takao,Kuo, Sheng-Chu

, p. 265 - 275 (2007/10/03)

As part of a continuing search for potential anticancer drug candidates in the 2-phenyl-4-quinolone series, 3′,6-substituted 2-phenyl-4-quinolone-3- carboxylic acid derivatives and their salts were synthesized and evaluated. Preliminary screening showed t

Substituted 2-phenyl-4-quinolone-3-carboxylic acid compounds and their use as antitumor agents

-

Page/Page column 5, (2008/06/13)

Substituted 2-phenyl-4-quinolone-3-carboxylic acid derivatives and their salts were synthesized. The results of preliminary screening revealed that these compounds are potent in killing solid tumor cancers.

Antimycobacterial activity of 3'- and 4'-fluorothiobenzanilides

Waisser,Kunes,Odlerova,Roman,Kubicova,Horak

, p. 193 - 195 (2007/10/03)

On the basis of a preliminary study of the antimycobacterial activity of thiobenzanilides, a group of 3/-fluoro- and 4/fluorothiobenzanilides has been synthesized and tested against Mycobacterium tuberculosis, M. kansasii, M. avium and M. fortuitum. The r

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