1220515-72-9

Basic information

• Product Name: 3-(diphenylamino)-2-iodocyclohex-2-enone
• Synonyms: 3-(diphenylamino)-2-iodocyclohex-2-enone
• CAS NO: 1220515-72-9
• Molecular Weight: 389.236
• Mol File: 1220515-72-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(diphenylamino)-2-iodocyclohex-2-enone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(diphenylamino)-2-iodocyclohex-2-enone(1220515-72-9)
• EPA Substance Registry System: 3-(diphenylamino)-2-iodocyclohex-2-enone(1220515-72-9)

Safety Data

• Hazardous Substances Data: 1220515-72-9(Hazardous Substances Data)

Upstream product

• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 24706-50-1 3-phenylaminocyclohex-2-enone 
• 504-02-9 1,3-cylohexanedione 
• 62-53-3 aniline 
• 122-39-4 diphenylamine 

Downstream Products

• 41175-15-9 9-phenyl-1,2,3,9-tetrahydro-4H-carbazol-4-one 
• 107396-23-6 N-(3-hydroxyphenyl)-diphenylamine 

Relevant articles and documents

Formation of 3-Aminophenols from Cyclohexane-1,3-diones

meta-Aminophenols are formed by the action of DBU on 3-amino-2-chlorocyclohex-2-en-1-ones at room temperature in MeCN. The chloro compounds are generated by treating 3-aminocyclohex-2-en-1-ones with the easily prepared halogenating agent BnNMe3·ICl2 in Me

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.