129603-19-6

Basic information

• Product Name: (S)-2-methyl-4-aminononane hydrochloride
• CAS NO: 129603-19-6
• Molecular Weight: 193.76
• Mol File: 129603-19-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-2-methyl-4-aminononane hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-methyl-4-aminononane hydrochloride(129603-19-6)
• EPA Substance Registry System: (S)-2-methyl-4-aminononane hydrochloride(129603-19-6)

Safety Data

• Hazardous Substances Data: 129603-19-6(Hazardous Substances Data)

Upstream product

• 116662-96-5 (2R)-2-(1,1-dimethylethoxycarbonylamino)-4-methylpentanal 
• 129603-01-6 (R)-N^α-(tert-butoxycarbonyl)-N-methoxy-N-methylleucinamide 
• 200937-21-9 (R)-Boc-leucine hydrate 
• 129603-07-2 ((Z)-(R)-1-Isobutyl-hex-2-enyl)-carbamic acid tert-butyl ester 
• 131064-84-1 ((E)-(R)-1-Isobutyl-hex-2-enyl)-carbamic acid tert-butyl ester 
• 129603-13-0 (S)-2-methyl-4-(tert. butoxycarbonylamino)nonane 

Relevant articles and documents

A Convenient and Versatile Synthesis of Chiral Aliphatic and Allylic Amines

Preparation of optically pure aliphatic and allylic amines from amino acids is described.Wittig olefination of α-Boc-amino aldehydes affords Boc-prodected allylic amines which can be deprotected to the corresponding chiral unsaturated amines.Catalytic reduction of the Wittig product prior to deprotection affords aliphatic amines of high optical purity.