503433-71-4

Basic information

• Product Name: (4RS,5R,8S)-4-benzyloxy-5,8-methano-5,9,9-trimethyl-1,2,3,4,5,6,7,8-octahydroacridine
• CAS NO: 503433-71-4
• Molecular Weight: 347.5
• Mol File: 503433-71-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4RS,5R,8S)-4-benzyloxy-5,8-methano-5,9,9-trimethyl-1,2,3,4,5,6,7,8-octahydroacridine(CAS DataBase Reference)
• NIST Chemistry Reference: (4RS,5R,8S)-4-benzyloxy-5,8-methano-5,9,9-trimethyl-1,2,3,4,5,6,7,8-octahydroacridine(503433-71-4)
• EPA Substance Registry System: (4RS,5R,8S)-4-benzyloxy-5,8-methano-5,9,9-trimethyl-1,2,3,4,5,6,7,8-octahydroacridine(503433-71-4)

Safety Data

• Hazardous Substances Data: 503433-71-4(Hazardous Substances Data)

Upstream product

• 157239-03-7 (1R,4S)-3-hydroxymethylene-1,7,7-trimethylbicyclo<2.2.1>heptan-2-one 
• 20618-41-1 (+)-3-hydroxymethylcamphor 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 36713-55-0 (±)-2-benzyloxycyclohexanone 
• 16161-84-5 <1R-(1β,4β)>-3-methylene-1,7,7-trimethylbicyclo<2.2.1>heptan-2-one 

Relevant articles and documents

Synthesis of chiral C2-symmetric 1,10-phenanthrolines from naturally occurring monoterpenes

A convenient procedure for the preparation of chiral C2-symmetric 1,10-phenanthrolines bearing a chiral framework in the form of a cycloalkeno-condensed substituent in the 2,3- and 8,9-positions of the heterocycle is reported. Starting from the 2-benzyloxycyclohexanone, four 1,10-phenanthrolines derived from (-)-β-pinene, (+)-α-pinene, (-)-isopinocampheol, and (+)-camphor were prepared according to a method based on a double Michael-azaannulation-aromatization sequence.