477498-68-3

Basic information

• Product Name: N-[2-(benzo[d]oxazol-2-yl)phenyl]cyclopropanecarboxamide
• Synonyms: N-[2-(benzo[d]oxazol-2-yl)phenyl]cyclopropanecarboxamide
• CAS NO: 477498-68-3
• Molecular Weight: 278.31
• Mol File: 477498-68-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[2-(benzo[d]oxazol-2-yl)phenyl]cyclopropanecarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(benzo[d]oxazol-2-yl)phenyl]cyclopropanecarboxamide(477498-68-3)
• EPA Substance Registry System: N-[2-(benzo[d]oxazol-2-yl)phenyl]cyclopropanecarboxamide(477498-68-3)

Safety Data

• Hazardous Substances Data: 477498-68-3(Hazardous Substances Data)

Upstream product

• 333349-66-9 2-iodo-N-(2-iodophenyl)benzamide 
• 6228-73-5 Cyclopropancarbamid 

Relevant articles and documents

One-pot tandem synthesis of 2-arylbenzoxazole derivatives via copper-catalyzed C-N and C-O bond formation

The reaction of 2-(2-halophenyl)halobenzamides with a series of nitrogen nucleophiles resulted in the formation of benzoxazole derivatives. This procedure involves copper-catalyzed one-pot tandem C-N/C-O coupling reactions. No ligand was used in the reaction, even in the cases of primary or secondary amides, which were used as N-nucleophiles. However, L-proline was used as ligand in the case of N-aromatic heterocycles like indole, imidazole and pyrazole derivatives. Copyright