79606-54-5

Basic information

• Product Name: N-<1-(1-adamantyl)ethylidene>cyclohexylamine
• Synonyms: N-<1-(1-adamantyl)ethylidene>cyclohexylamine
• CAS NO: 79606-54-5
• Molecular Weight: 259.435
• Mol File: 79606-54-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-<1-(1-adamantyl)ethylidene>cyclohexylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-<1-(1-adamantyl)ethylidene>cyclohexylamine(79606-54-5)
• EPA Substance Registry System: N-<1-(1-adamantyl)ethylidene>cyclohexylamine(79606-54-5)

Safety Data

• Hazardous Substances Data: 79606-54-5(Hazardous Substances Data)

Upstream product

• 1660-04-4 1-acetyladamantane 
• 108-91-8 cyclohexylamine 

Downstream Products

• 79606-58-9 N-methyl-N-cyclohexyladamantane-carboxamide 
• 81311-58-2 N-cyclohexyladamantane-1-carboxamide 
• 79606-56-7 2-cyclohexyl-3-(1-adamantyl)-3-methyloxaziridine 

Relevant articles and documents

SYNTHESIS AND TRANSFORMATIONS OF OXAZIRIDINES. ADAMANTANE-2-SPIRO-3'-OXAZIRIDINE AND ITS N-ALKYL DERIVATIVES

Unsubstituted and N-substituted adamantane-2-spiro-3'-oxaziridine were synthesized by the oxidation of Schiff bases, obtained from adamantanone and alkyl(aryl)amines, with peroxyacetic acid.The thermal rearrangement of the N-substituted derivatives leads to N-substituted 5-azahomoadamantan-4-ones, while fragmentation under the influence of Fe(II) ions leads to derivatives of bicyclononane in the form of N-substituted amides.Adamantane-2-spiro-3'-oxaziridine gives different transformation products, i.e., adamantanone in the first case and 5-azahomoadamantan-4-one in the second.