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N-(4-chlorophenyl)-2-fluorobenzamide is a chemical compound with the molecular formula C13H9ClFNO. It is a derivative of benzamide, featuring a 4-chlorophenyl group attached to the nitrogen atom and a fluorine atom on the benzene ring. N-(4-chlorophenyl)-2-fluorobenzamide is known for its potential applications in the field of pharmaceuticals and agrochemicals, particularly as a precursor in the synthesis of various active ingredients. Its structure allows for the exploration of its properties and reactivity, which can be crucial in the development of new drugs or pesticides. The specific combination of chlorine and fluorine atoms in the molecule can influence its electronic properties and biological activity, making it a subject of interest for researchers in medicinal chemistry and related fields.

784-65-6

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784-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 784-65-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 784-65:
(5*7)+(4*8)+(3*4)+(2*6)+(1*5)=96
96 % 10 = 6
So 784-65-6 is a valid CAS Registry Number.

784-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-N-(4-chlorophenyl)benzamide

1.2 Other means of identification

Product number -
Other names 2-Fluor-benzoesaeure-(4-chlor-anilid)

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:784-65-6 SDS

784-65-6Relevant 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

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

-

Page/Page column 6, (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.

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