1220516-02-8

Basic information

• Product Name: methyl 4-[benzyl(2-iodo-3-oxocyclohex-1-enyl)amino]benzoate
• Synonyms: methyl 4-[benzyl(2-iodo-3-oxocyclohex-1-enyl)amino]benzoate
• CAS NO: 1220516-02-8
• Molecular Weight: 461.299
• Mol File: 1220516-02-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 4-[benzyl(2-iodo-3-oxocyclohex-1-enyl)amino]benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-[benzyl(2-iodo-3-oxocyclohex-1-enyl)amino]benzoate(1220516-02-8)
• EPA Substance Registry System: methyl 4-[benzyl(2-iodo-3-oxocyclohex-1-enyl)amino]benzoate(1220516-02-8)

Safety Data

• Hazardous Substances Data: 1220516-02-8(Hazardous Substances Data)

Upstream product

• 16307-38-3 (4-(methoxycarbonyl)phenyl)-λ³-iodanediyl diacetate 
• 41609-04-5 N-benzyl-3-amino-2-cyclohexen-1-one 
• 100-46-9 benzylamine 
• 504-02-9 1,3-cylohexanedione 

Downstream Products

• 1396649-82-3 methyl 9-benzyl-4-oxo-2,3,4,9-tetrahydro-1H-carbazole-6-carboxylate 

Relevant articles and documents

Synthesis of N-substituted carbazolones from α-iodo enaminones via Pd(0)-catalyzed intramolecular coupling under microwave irradiation

A variety of N-aryl and N-alkyl carbazolones were conveniently achieved in good to high yields via Pd2(dba)3-mediated intramolecular coupling of N-substituted α-iodo enaminones under microwave irradiation. The Pd(0)-catalyzed cyclization was found to proceed favorably with the more electron-deficient phenyl ring during the reactions involving unsymmetrical N,N-diaryl α-iodo enaminones. This unique property enables the construction of carbazolone skeleton containing nitro substituted benzenoid ring.