34999-46-7

Basic information

• Product Name: N-(2-(4-fluorobenzoyl)-4-chlorophenyl)acetamide
• CAS NO: 34999-46-7
• Molecular Weight: 291.709
• Mol File: 34999-46-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(2-(4-fluorobenzoyl)-4-chlorophenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(4-fluorobenzoyl)-4-chlorophenyl)acetamide(34999-46-7)
• EPA Substance Registry System: N-(2-(4-fluorobenzoyl)-4-chlorophenyl)acetamide(34999-46-7)

Safety Data

• Hazardous Substances Data: 34999-46-7(Hazardous Substances Data)

Upstream product

• 7033-50-3 6-chloro-2-methyl-4H-benzo[d][1,3]oxazin-4-one 
• 352-13-6 4-flourophenylmagnesium bromide 
• 459-57-4 4-fluorobenzaldehyde 
• 539-03-7 N-(4-chlorophenyl)acetamide 

Downstream Products

• 35001-86-6 6-chloro-4-(4-fluoro-phenyl)-1,4-dihydro-benzo[d][1,3]thiazine-2-thione 
• 35001-98-0 6-chloro-4-(4-fluoro-phenyl)-2-methylsulfanyl-4H-benzo[d][1,3]thiazine 
• 16771-51-0 (2-amino-5-chloro-phenyl)-(4-fluoro-phenyl)-methanol 
• 784-40-7 (2-amino-5-chlorophenyl)(4-fluorophenyl)methanone 

Relevant articles and documents

Activation of C-H Activation: The Beneficial Effect of Catalytic Amount of Triaryl Boranes on Palladium-Catalyzed C-H Activation

Herein we report a novel approach to the acceleration of palladium-catalyzed C-H activation reactions. We demonstrated that the utilization of electron-deficient triaryl boranes as Lewis acidic cocatalysts of palladium enables the directed cross dehydrogenative coupling of aldehydes and anilides under mild reaction conditions. Study of the kinetic profile of the transformation reveals a unique, unexpectedly long induction period of the transformation.