129397-36-0

Basic information

• Product Name: N-(2-cyclohexylethylidene)-(S)-α-methylbenzylamine
• Synonyms: N-(2-cyclohexylethylidene)-(S)-α-methylbenzylamine
• CAS NO: 129397-36-0
• Molecular Weight: 229.365
• Mol File: 129397-36-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(2-cyclohexylethylidene)-(S)-α-methylbenzylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-cyclohexylethylidene)-(S)-α-methylbenzylamine(129397-36-0)
• EPA Substance Registry System: N-(2-cyclohexylethylidene)-(S)-α-methylbenzylamine(129397-36-0)

Safety Data

• Hazardous Substances Data: 129397-36-0(Hazardous Substances Data)

Upstream product

• 2627-86-3 (S)-1-phenyl-ethylamine 
• 2043-61-0 cyclohexanecarbaldehyde 
• 3289-28-9 ethyl cyclohexanecarboxylate 
• 5664-21-1 cyclohexylacetaldehyde 
• 5452-75-5 ethyl 2-cyclohexylacetate 

Downstream Products

• 155748-65-5 methyl (2R,3S)-2-hydroxy-4-c-hexyl-3-<(S)-1-methylbenzylamino>butanoate 
• 129397-39-3 3-benzyloxy-4-cyclohexylmethyl-1-<(S)-1-phenylethyl>-2-azetidinone 
• 121506-22-7 (2R,3S)-nor-C-statine hydrochloride 

Relevant articles and documents

A Stereoselective Synthesis of the (2R,3S)- and (2S,3R)-3-Amino-2-hydroxybutyric Acid Derivatives, the Key Components of a Renin Inhibitor and Bestatin

The title synthesis was achieved by featuring the -cycloaddition reaction of benzyloxyketene with a chiral imine derived from methyl (R)- or (S)-mandelate, alcoholysis of the formed 3,4-cis disubstituted β-lactam under acidic conditions, and reductiv