135028-69-2

Basic information

• Product Name: (1S,2S)-1-Methyl-2-phenyl-2-((1R,2R,4S,6R,7R)-1,10,10-trimethyl-3-oxa-tricyclo[5.2.1.0^2,6]dec-4-yloxy)-ethylamine
• CAS NO: 135028-69-2
• Molecular Weight: 329.483
• Mol File: 135028-69-2.mol

Chemical Properties

• CAS DataBase Reference: (1S,2S)-1-Methyl-2-phenyl-2-((1R,2R,4S,6R,7R)-1,10,10-trimethyl-3-oxa-tricyclo[5.2.1.0^2,6]dec-4-yloxy)-ethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-1-Methyl-2-phenyl-2-((1R,2R,4S,6R,7R)-1,10,10-trimethyl-3-oxa-tricyclo[5.2.1.0^2,6]dec-4-yloxy)-ethylamine(135028-69-2)
• EPA Substance Registry System: (1S,2S)-1-Methyl-2-phenyl-2-((1R,2R,4S,6R,7R)-1,10,10-trimethyl-3-oxa-tricyclo[5.2.1.0^2,6]dec-4-yloxy)-ethylamine(135028-69-2)

Safety Data

• Hazardous Substances Data: 135028-69-2(Hazardous Substances Data)

Upstream product

• 532-28-5 (RS)-mandelonitrile 
• 108031-76-1 <2R-(2α,3aα,4β,7β,7aα)>-Octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-ol 

Downstream Products

• 3198-15-0 (1R,2S)-(-)-norephedrine hydrochloride 

Relevant articles and documents

Amino-Alcohols, I: A Method for the Synthesis of Enantiomerically Pure 1,2-Aminoalcohols with erythro-Configuration

The synthesis of both enantiomers of norephedrine and norisoephedrine is described to present a method for the preparation of enantiomerically pure branched 1,2-aminoalcohols.In a one pot reaction enantiomerically pure cyanohydrins bearing an acetal protective group are subjected to Grignard-reaction followed by addition of lithium aluminium hydride.After deprotection the target compounds are obtained.