1402836-42-3

Basic information

• Product Name: 7-methyl-2-(4-methylphenyl)-2,3-dihydrobenzo[e][1,4]oxazepin-5(1H)-one
• Synonyms: 7-methyl-2-(4-methylphenyl)-2,3-dihydrobenzo[e][1,4]oxazepin-5(1H)-one
• CAS NO: 1402836-42-3
• Molecular Weight: 267.327
• Mol File: 1402836-42-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 7-methyl-2-(4-methylphenyl)-2,3-dihydrobenzo[e][1,4]oxazepin-5(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-methyl-2-(4-methylphenyl)-2,3-dihydrobenzo[e][1,4]oxazepin-5(1H)-one(1402836-42-3)
• EPA Substance Registry System: 7-methyl-2-(4-methylphenyl)-2,3-dihydrobenzo[e][1,4]oxazepin-5(1H)-one(1402836-42-3)

Safety Data

• Hazardous Substances Data: 1402836-42-3(Hazardous Substances Data)

Upstream product

• 42107-37-9 α-chloro-p-methylstyrene 
• 124-38-9 carbon dioxide 
• 106-49-0 p-toluidine 
• 2941-78-8 2-Amino-5-methylbenzoic acid 
• 13107-39-6 2-(4-methylphenyl)oxirane 

Relevant articles and documents

Facile synthesis for benzo-1,4-oxazepine derivatives by tandem transformation of C-N coupling/C-H carbonylation

A tandem transformation of C-N coupling/C-H carbonylation has been developed for the synthesis of benzo-1,4-oxazepine pharmaceutically derivatives. Notably, this reaction was accomplished by various phenylamine with ally halides under carbon dioxide atmosphere employing 2-(2-dimethylamino-vinyl)-1H-inden-1-olcatalyzed. Furthermore, under the optimized conditions, various benzo-1,4-oxazepine derivatives were obtained in good yields. Finally, a plausible CuI/CuIII mechanism of C-N coupling/C-H carbonylation transformation was proposed.