56037-35-5

Basic information

• Product Name: Benzenamine, N-(1-cyclohexylethylidene)-, (E)-
• CAS NO: 56037-35-5
• Molecular Formula: C14H19N
• Molecular Weight: 201.312
• Mol File: 56037-35-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-(1-cyclohexylethylidene)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-(1-cyclohexylethylidene)-, (E)-(56037-35-5)
• EPA Substance Registry System: Benzenamine, N-(1-cyclohexylethylidene)-, (E)-(56037-35-5)

Safety Data

• Hazardous Substances Data: 56037-35-5(Hazardous Substances Data)

Upstream product

• 931-48-6 2-cyclohexylacetylene 
• 62-53-3 aniline 
• 823-76-7 Cyclohexyl methyl ketone 
• 100-63-0 phenylhydrazine 

Downstream Products

• 58008-17-6 N-phenyl-1-cyclohexylethylamine 

Relevant articles and documents

L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: Effects of the side amide group on catalytic performances

A series of N-formamides derived from pipecolinic acid have been synthesized and tested as Lewis base catalysts for the enantioselective reduction of N-aryl imines by trichlorosilane. Through the investigation of the structure-efficacy relationship between the side amide group and catalytic performance, several highly effective catalysts were discovered. In particular, arylamido-type catalyst 5i and non-arylamido-type catalyst 6c exhibited high reactivity and enantioselectivity, furnishing the reduction of a wide variety of N-aryl imines with high isolated yields (up to 98%) and ee values (up to 96%) under mild conditions. Moreover, these two catalysts complement each other in terms of their tolerances to nonaromatic ketimines and non-methyl ketimines. The Royal Society of Chemistry 2013.

L-piperazine-2-carboxylic acid derived N-formamide as a highly enantioselective Lewis basic catalyst for hydrosilylation of N-aryl imines with an unprecedented substrate profile

L-Piperazine-2-carboxylic acid derived N-formamides have been developed as highly enantioselective Lewis basic catalysts for the hydrosilylation of N-aryl imines with trichlorosilane. The arene sulfonyl group on N4 was found to be critical for the high en

A highly enantioselective Lewis basic organocatalyst for reduction of N-aryl imines with unprecedented substrate spectrum

L-Pipecolinic acid derived formamides have been developed as highly efficient and enantioselective Lewis basic organocatalysts for the reduction of N-aryl imines with trichlorosilane. Catalyst 4b afforded high isolated yields (up to 98%) and enantioselect