74708-32-0

Basic information

• Product Name: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide
• CAS NO: 74708-32-0
• Molecular Weight: 311.424
• Mol File: 74708-32-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide(74708-32-0)
• EPA Substance Registry System: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide(74708-32-0)

Safety Data

• Hazardous Substances Data: 74708-32-0(Hazardous Substances Data)

Upstream product

• 74708-24-0 (1R*,2S*)-2-hydroxycyclohexane acetonitrile 
• 24871-12-3 trans-hexahydro-2(3H)-benzofuranone 
• 74629-95-1 (1R,2S,R)-cis-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide 
• 74629-97-3 (1R,2R,R)-trans-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-Naphthyl)ethyl>amide 
• 74629-96-2 (1S,2S,R)-trans-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide 
• 74629-94-0 (1S,2R,R)-cis-1-(2-Hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl N-<1-(1-naphthyl)ethyl>amide 
• 42185-27-3 2-(cyanomethyl)cyclohexanone 
• 3886-70-2 (R)-1-(1-Naphthyl)ethylamine 
• 6051-03-2 cis-hexahydrobenzofuran-2(3H)-one 

Relevant articles and documents

Enantiomerically Pure Lactones. 2. Approaches to Cis or Trans Multicyclic Lactones

Enantiomerically pure bicyclic lactones 1-3 and tricyclic lactones 4 and 5 have been prepared by either of two procedures, each hinging upon the liquid chromatographic seperation of rationally selected diastereomeric derivatives.After seperation, the diastereomers are converted by a simple high-yield reaction sequence to the enantiomeric multiring lactones, none of which has been previously reported in optically active form. The relative strengths and weaknesses of each approach are discussed.Lactones 4 and 5 were α-methylated, these derivatives being suitable for the determination of enantiomeric purity and absolute configuration using the chiral solvating agent (S)-(+)-2,2,2-trifluoro-1-(9-anthryl)ethanol.