22303-86-2

Basic information

• Product Name: (4-Chloro-phenyl)-cyclohex-1-enyl-amine
• Synonyms: (4-Chloro-phenyl)-cyclohex-1-enyl-amine
• CAS NO: 22303-86-2
• Molecular Weight: 207.703
• Mol File: 22303-86-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-Chloro-phenyl)-cyclohex-1-enyl-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (4-Chloro-phenyl)-cyclohex-1-enyl-amine(22303-86-2)
• EPA Substance Registry System: (4-Chloro-phenyl)-cyclohex-1-enyl-amine(22303-86-2)

Safety Data

• Hazardous Substances Data: 22303-86-2(Hazardous Substances Data)

Upstream product

• 125519-72-4 N-(1-cyclohexen-1-yl)-N-(trimethylsilyl)-4-chloroaniline 
• 106-47-8 4-chloro-aniline 
• 108-94-1 cyclohexanone 
• 1165952-91-9 cyclohexa-1,3-diene 
• 36132-64-6 N-(cyclohexylidine)-4-chloro-aniline 

Downstream Products

• 108-94-1 cyclohexanone 
• 106-47-8 4-chloro-aniline 

Relevant articles and documents

Hydroamination of 1,3-cyclohexadiene with aryl amines catalyzed with acidic form zeolites

The intermolecular hydroamination of 1,3-cyclohexadiene with aniline using zeolite catalysts was investigated. The reaction mechanism and the influence of amine basicity on the rate of reaction were studied. Zeolite H-BEA was the most active catalyst, whereas the incorporation of Zn2+ (Zn/H-BEA) led to decreasing catalytic activity, indicating that the reaction is catalyzed by Bronsted acid sites. Subtle shape selective effects determine the reactivity and selectivity of the zeolites.

Imine-enamine tautomerism in the anils of cyclohexanone and 2-(β-cyanoethyl)cyclohexanone

The products from the condensation of cyclohexanone and 2-(β-cyanoethyl)cyclohexanone with para- and ortho-disubstituted anilines in 10percent solutions in carbon tetrachloride exist as mixtures of the imine and enamine tautomers.The tautomeric compositio