84619-58-9

Basic information

• Product Name: (S)-(+)-1-amino-(1-cyclohexyl)ethanol
• Synonyms: (S)-(+)-1-amino-(1-cyclohexyl)ethanol
• CAS NO: 84619-58-9
• Molecular Weight: 143.229
• Mol File: 84619-58-9.mol

Chemical Properties

• CAS DataBase Reference: (S)-(+)-1-amino-(1-cyclohexyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-1-amino-(1-cyclohexyl)ethanol(84619-58-9)
• EPA Substance Registry System: (S)-(+)-1-amino-(1-cyclohexyl)ethanol(84619-58-9)

Safety Data

• Hazardous Substances Data: 84619-58-9(Hazardous Substances Data)

Upstream product

• 362519-24-2 (S)-(+)-hexahydromandelamide 
• 362519-23-1 (S)-(-)-2,2-dimethyl-5-cyclohexyl-1,3-dioxolan-4-one 
• 61475-31-8 (S)-hexahydromandelic acid 
• 357952-91-1 (S)-(+)-1-Cyclohexyl-2-(p-tolylsulfonyloxy)ethanol 

Relevant articles and documents

Application of optically active 1,2-diol monotosylates for synthesis of β-azido and β-amino alcohols with very high enantiomeric purity. Synthesis of enantiopure (R)-octopamine, (R)-tembamide and (R)-aegeline

A very convenient and highly efficient synthesis of near enantiopure β-azido and β-amino alcohols including biologically active substances such as (R)-octopamine, (R)-tembamide and (R)-aegeline from optically active 1,2-diol monotosylates is reported.

1,1′-Binaphthylazepine-based ligands for asymmetric catalysis. Part 1: Preparation and characterization of some new aminoalcohols and diamines

Starting from (S)-1,1′-binaphthol, a series of ten novel enantiopure 1,1′-binaphthylazepine-based aminoalcohols and diamines 1a-1j were efficiently prepared and fully characterized. These derivatives, having either only an atropisomeric bridged-binaphthyl backbone or an additional stereogenic carbon center, can be interesting ligands for asymmetric catalysis.