1334324-63-8

Basic information

• Product Name: N-Cbz-L-2-aMino-2-cyclohexyl-ethanol
• Synonyms: N-Cbz-L-2-aMino-2-cyclohexyl-ethanol;Cbz-L-Chg-OL
• CAS NO: 1334324-63-8
• Molecular Formula: C16H23NO3
• Molecular Weight: 277.35872
• Mol File: 1334324-63-8.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Cbz-L-2-aMino-2-cyclohexyl-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: N-Cbz-L-2-aMino-2-cyclohexyl-ethanol(1334324-63-8)
• EPA Substance Registry System: N-Cbz-L-2-aMino-2-cyclohexyl-ethanol(1334324-63-8)

Safety Data

• Hazardous Substances Data: 1334324-63-8(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 1217341-09-7 C₁₇H₂₇NO₂ 
• 1403991-13-8 C₁₆H₂₁NO₃ 
• 1070268-86-8 benzyl 1-cyclohexyl-2,2-dimethoxyethylcarbamate 
• 1072409-66-5 1-cyclohexyl-2,2-dimethoxyethylamine 
• 69901-75-3 (S)-[[(benzyloxy)carbonyl]amino](cyclohexyl)acetic acid 

Relevant articles and documents

Resolution and absolute configuration of some a-aminoacetals: En route to enantiopure N-protected a-aminoaldehydes

The first successful resolution of rac-a-aminoacetals via diastereoisomeric salt formation with optically pure N-protected aminoacids is reported. The absolute configuration assignment of a-aminoacetal enantiomers is performed by an entirely non-racemizing chemical correlation method involving N-protection and a new efficient hydrolysis step followed by a reduction of the resulting N-protected a-aminoaldehyde intermediates. A racemization method of optically enriched a-aminoacetals is exemplified to allow valorisation of both enantiomers. Springer-Verlag 2011.