162355-99-9

Basic information

• Product Name: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide
• Synonyms: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide
• CAS NO: 162355-99-9
• Molecular Weight: 235.37
• Mol File: 162355-99-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide(162355-99-9)
• EPA Substance Registry System: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide(162355-99-9)

Safety Data

• Hazardous Substances Data: 162355-99-9(Hazardous Substances Data)

Upstream product

• 162356-10-7 trans N-<3-(pent-2-enyl)> trichloroacetamide 
• 108-94-1 cyclohexanone 
• 79-30-1 isobutyryl chloride 
• 51616-90-1 (+/-)-(E)-1-methyl-2-butenylamine 

Downstream Products

• 162356-02-7 Cyclohex-1-enyl-isobutyl-((E)-1-methyl-but-2-enyl)-amine 

Relevant articles and documents

Stereochemical consequences of the Lewis acid-promoted 3-aza-cope rearrangement of N-alkyl-N-allyl enamines

Internal and relative asymmetric induction were examined for the electrophile promoted 3-aza-Cope rearrangement of substituted N-alkyl-N-allyl enamines. In general, internal asymmetric induction was highly variable, and was dependent both upon the nature