113350-24-6

Basic information

• Product Name: [(1S,2S)-2-((1S,3S)-3-Hydroxy-1-methyl-butoxy)-1-isobutyl-pent-4-enyl]-carbamic acid benzyl ester
• CAS NO: 113350-24-6
• Molecular Weight: 377.524
• Mol File: 113350-24-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(1S,2S)-2-((1S,3S)-3-Hydroxy-1-methyl-butoxy)-1-isobutyl-pent-4-enyl]-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(1S,2S)-2-((1S,3S)-3-Hydroxy-1-methyl-butoxy)-1-isobutyl-pent-4-enyl]-carbamic acid benzyl ester(113350-24-6)
• EPA Substance Registry System: [(1S,2S)-2-((1S,3S)-3-Hydroxy-1-methyl-butoxy)-1-isobutyl-pent-4-enyl]-carbamic acid benzyl ester(113350-24-6)

Safety Data

• Hazardous Substances Data: 113350-24-6(Hazardous Substances Data)

Upstream product

• 113283-61-7 benzyl (S)-1-isobutyl-2,2-dimethoxyethylcarbamate 
• 113283-74-2 [(S)-1-((4S,6S)-4,6-Dimethyl-[1,3]dioxan-2-yl)-3-methyl-butyl]-carbamic acid benzyl ester 
• 762-72-1 allyl-trimethyl-silane 

Relevant articles and documents

Asymmetric Synthesis of 2- Amino Alcohol Derivatives from (S)-α-Amino Aldehydes via Acetal Templates

Titanium tetrachloride mediated addition of allyltrimethylsilane to chiral acetals derived from (S)-α-amino aldehydes and (+)-(2S,4S)-pentane-2,4-diol gave the anti-2-amino alcohol derivatives with considerably high diastereoselectivity.On the other hand,