287488-25-9

Basic information

• Product Name: Bicyclo[2.2.1]heptan-2-imine, 1,7,7-trimethyl-, (1R,4R)- (9CI)
• Synonyms: Bicyclo[2.2.1]heptan-2-imine, 1,7,7-trimethyl-, (1R,4R)- (9CI)
• CAS NO: 287488-25-9
• Molecular Formula: C₁₀H₁₇N
• Molecular Weight: 151.24868
• Product Categories: CYCLOPENTANE
• Mol File: 287488-25-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bicyclo[2.2.1]heptan-2-imine, 1,7,7-trimethyl-, (1R,4R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Bicyclo[2.2.1]heptan-2-imine, 1,7,7-trimethyl-, (1R,4R)- (9CI)(287488-25-9)
• EPA Substance Registry System: Bicyclo[2.2.1]heptan-2-imine, 1,7,7-trimethyl-, (1R,4R)- (9CI)(287488-25-9)

Safety Data

• Hazardous Substances Data: 287488-25-9(Hazardous Substances Data)

Upstream product

• 2792-42-9 (R,R)-camphor oxime 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 1191099-59-8 (1R,4R)-1-oxo-2-(1,7,7-trimethylbicyclo[2.2.1]hept-2-ylidene)-hydrazinium-1-olate 
• 31180-79-7 N-nitrocaphorimine 

Downstream Products

• 287488-39-5 spiro[(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,5'-(phenyl)-1,4',2'-dioxazole] 
• 122270-27-3 spiro[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3'-N-phenylsulfonyloxaziridine] 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 113723-87-8 tert-butyl (R)-3'-phenyl-2'-([1R,2E,4R]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ylideneamino)propanoate 
• 334817-48-0 tert-butyl (S)-3'-phenyl-2'-([1R,2E,4R]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ylideneamino)propanoate 
• 334817-46-8 methyl (S)-3'-phenyl-2'-([1R,2E,4R]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ylideneamino)propanoate 
• 76-22-2 Camphor 

Relevant articles and documents

Studies on the preparation of camphorylidene derivatives of α-amino acids

An improved method has been developed for the efficient synthesis of stable camphor imine salts. Camphor imine readily undergoes transimination with α-amino acid ester hydrochlorides to yield camphorylidene amino acid derivatives with E stereochemistry about the C=N double bond. Sodium cyanoborohydride reduction of the derived ketimines gives exo-bornylamines.