33341-64-9

Basic information

• Product Name: Benzamide, N,4-dichloro-
• CAS NO: 33341-64-9
• Molecular Formula: C7H5Cl2NO
• Molecular Weight: 190.029
• Mol File: 33341-64-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzamide, N,4-dichloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N,4-dichloro-(33341-64-9)
• EPA Substance Registry System: Benzamide, N,4-dichloro-(33341-64-9)

Safety Data

• Hazardous Substances Data: 33341-64-9(Hazardous Substances Data)

Upstream product

• 619-56-7 4-chlorobenzamide 

Downstream Products

• 1346684-68-1 6-chloro-2,3-diphenylisoquinolin-1-(2H)-one 
• 76047-46-6 2-[3-(4-Chloro-phenyl)-[1,2,4]oxadiazol-5-yl]-1-(4-trifluoromethyl-phenyl)-ethanone 
• 76047-50-2 2-[3-(4-Chloro-phenyl)-[1,2,4]oxadiazol-5-yl]-1-(4-dimethylamino-phenyl)-ethanone 
• 76047-37-5 3-(p-chlorophenyl)-5-(β-amino-p-methoxyphenacyl)-1,2,4-oxadiazole 
• 76047-47-7 1-(4-Chloro-phenyl)-2-[3-(4-chloro-phenyl)-[1,2,4]oxadiazol-5-yl]-ethanone 
• 76047-36-4 3-(p-chlorophenyl)-5-(β-amino-p-methylphenacyl)-1,2,4-oxadiazole 
• 115665-17-3 [3-(4-Chloro-phenyl)-5-phenyl-isoxazol-4-yl]-(4-methoxy-phenyl)-methanone 
• 115665-14-0 (4-Chloro-phenyl)-[3-(4-chloro-phenyl)-5-phenyl-isoxazol-4-yl]-methanone 
• 115665-10-6 3-(4-Chloro-phenyl)-5-(4-methoxy-phenyl)-isoxazole-4-carboxylic acid methyl ester 
• 115665-07-1 3,5-Bis-(4-chloro-phenyl)-isoxazole-4-carboxylic acid methyl ester 
• 115665-23-1 methyl 3-(4-chlorophenyl)-5-phenylisoxazole-4-carboxylate 
• 14764-45-5 [3-(4-chloro-phenyl)-5-phenyl-isoxazol-4-yl]-phenyl-methanone 
• 87446-72-8 trans-3-p-chlorophenyl-4-nitro-5-trichloromethyl-4,5-dihydro-1,2-oxazole 
• 91407-59-9 4-Chloro-N-[2-(4-chloro-phenyl)-6-phenyl-5,6-dihydro-4λ⁴-[1,4,3]oxathiazin-(4E)-ylidene]-benzamide 

Relevant articles and documents

Direct access to cobaltacycles via C-H activation: N-chloroamide- enabled room-temperature synthesis of heterocycles

Cobaltacycle synthesis via C-H activation has been achieved for the first time, providing key mechanistic insight into cobalt catalytic chemistry. NChloroamides are used as a directing synthon for cobalt-catalyzed roomtemperature C-H activation and construction of heterocycles. Alkynes as coupling partners allow convenient access to isoquinolones, a class of synthetically and pharmaceutically important compounds. The broad substrate scope enables a diverse range of substitution patterns to be incorporated into the heterocyclic scaffold.