58955-03-6

Basic information

• Product Name: Benzamide, 3-fluoro-N-(4-methoxyphenyl)-
• CAS NO: 58955-03-6
• Molecular Formula: C14H12FNO2
• Molecular Weight: 245.253
• Mol File: 58955-03-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzamide, 3-fluoro-N-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 3-fluoro-N-(4-methoxyphenyl)-(58955-03-6)
• EPA Substance Registry System: Benzamide, 3-fluoro-N-(4-methoxyphenyl)-(58955-03-6)

Safety Data

• Hazardous Substances Data: 58955-03-6(Hazardous Substances Data)

Upstream product

• 98-80-6 phenylboronic acid 
• 104-94-9 4-methoxy-aniline 
• 1711-07-5 3-fluorobenzoyl chloride 

Downstream Products

• 1325219-42-8 C₁₅H₁₄FNO₂S 
• 1186650-26-9 5-fluoro-2-(4-methoxyphenyl)benzo[d]isothiazol-3(2H)-one 
• 828264-14-8 2-[(3-fluoro-phenyl)-(4-methoxy-phenylamino)-methylene]-malonic acid diethyl ester 
• 828264-29-5 ethyl 3'-fluoro-6-methoxy-2-phenyl-4-quinolone-3-carboxylate 

Relevant articles and documents

Nickel-Catalyzed Denitrogenative Cross-Coupling Reaction of 1,2,3-Benzotriazin-4(3 H)-ones with Organoboronic Acids: An Easy Access to Ortho-Arylated and Alkenylated Benzamides

A novel nickel-catalyzed approach to synthesize ortho-arylated and alkenylated benzamides in good to high yields via a denitrogenative cross-coupling reaction of 1,2,3-benzotriazin-4(3H)-ones with organoboronic acids is described. The reaction proceeds th

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.