259817-06-6

Basic information

• Product Name: ethyl 2-diazo-3-[N-(4-methoxybenzoyl)-N-phenylamino]-3-oxopropanoate
• Synonyms: ethyl 2-diazo-3-[N-(4-methoxybenzoyl)-N-phenylamino]-3-oxopropanoate
• CAS NO: 259817-06-6
• Molecular Weight: 367.361
• Mol File: 259817-06-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 2-diazo-3-[N-(4-methoxybenzoyl)-N-phenylamino]-3-oxopropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-diazo-3-[N-(4-methoxybenzoyl)-N-phenylamino]-3-oxopropanoate(259817-06-6)
• EPA Substance Registry System: ethyl 2-diazo-3-[N-(4-methoxybenzoyl)-N-phenylamino]-3-oxopropanoate(259817-06-6)

Safety Data

• Hazardous Substances Data: 259817-06-6(Hazardous Substances Data)

Upstream product

• 57072-87-4 chlorocarbonyl-diazo-acetic acid ethyl ester 
• 7465-88-5 4-methoxy-N-phenylbenzamide 

Downstream Products

• 210837-59-5 5-ethoxycarbonyl-2-(4-methoxyphenyl)-3-phenyl-1,3-oxazolium-4-olate 

Relevant articles and documents

Organophosphorus compounds. Part 144: A novel approach to 1,3- oxaphospholes from phosphaalkynes and isomunchnones

Phosphaalkynes 5 react with the isomunchnones 12 in a regiospecific process to furnish the 1,3-oxaphospholes 14. In contrast to other cycloadditions to isomunchnones, the bicyclic intermediate 13 cannot be detected in these reactions. It is not necessary to use isolated isomunchnones 12 for the synthesis of the 1,3-oxaphospholes. The reaction sequence is also successful by use of the diazocarbonyl compounds 11 and in situ generation of the isomunchnones therefrom.