1978-87-6

Basic information

• Product Name: N-(4-chlorophenyl)-3-fluorobenzamide
• Synonyms: N-(4-chlorophenyl)-3-fluorobenzamide
• CAS NO: 1978-87-6
• Molecular Formula: C₁₃H₉ClFNO
• Molecular Weight: 249.6680632
• Mol File: 1978-87-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-chlorophenyl)-3-fluorobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-chlorophenyl)-3-fluorobenzamide(1978-87-6)
• EPA Substance Registry System: N-(4-chlorophenyl)-3-fluorobenzamide(1978-87-6)

Safety Data

• Hazardous Substances Data: 1978-87-6(Hazardous Substances Data)

Upstream product

• 637-87-6 1-Chloro-4-iodobenzene 
• 455-37-8 3-fluorobenzamide 
• 106-47-8 4-chloro-aniline 
• 1711-07-5 3-fluorobenzoyl chloride 

Downstream Products

• 1251912-87-4 C₁₃H₇ClFNOS 
• 1186646-43-4 2-(4-chlorophenyl)-5-fluorobenzo[d]isothiazol-3(2H)-one 
• 828264-11-5 2-[(4-chloro-phenylamino)-(3-fluoro-phenyl)-methylene]-malonic acid diethyl ester 
• 828264-26-2 ethyl 3'-fluoro-6-chloro-2-phenyl-4-quinolone-3-carboxylate 

Relevant articles and documents

Studies towards the design and synthesis of novel 1,5-diaryl-1h-imidazole-4-carboxylic acids and 1,5-diaryl-1h-imidazole-4-carbohydrazides as host ledgf/p75 and hiv-1 integrase interaction inhibitors

Two targeted sets of novel 1,5-diaryl-1H-imidazole-4-carboxylic acids 10 and carbohy-drazides 11 were designed and synthesized from their corresponding ester intermediates 17, which were prepared via cycloaddition of ethyl isocyanoacetate 16 and diarylimi

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

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

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.