854102-52-6

Basic information

• Product Name: [(S,E)-3-methyl-1-styrylbutyl]carbamic acid tert-butyl ester
• Synonyms: [(S,E)-3-methyl-1-styrylbutyl]carbamic acid tert-butyl ester
• CAS NO: 854102-52-6
• Molecular Weight: 289.418
• Mol File: 854102-52-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(S,E)-3-methyl-1-styrylbutyl]carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(S,E)-3-methyl-1-styrylbutyl]carbamic acid tert-butyl ester(854102-52-6)
• EPA Substance Registry System: [(S,E)-3-methyl-1-styrylbutyl]carbamic acid tert-butyl ester(854102-52-6)

Safety Data

• Hazardous Substances Data: 854102-52-6(Hazardous Substances Data)

Upstream product

• 75899-20-6 (C₅H₉O₂)(NHCHCOO)(CH₂C₃H₇)(CO₂C₂H₅) 
• 82010-31-9 (S)-(1-hydroxymethyl-3-methylbutyl)carbamic acid tert-butyl ester 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 58521-45-2 tert-butoxycarbonyl-L-leucinal 
• 1449-46-3 benzyltriphenylphosphonium bromide 

Downstream Products

• 146453-32-9 (R)-4-([(tert-butoxy)carbonyl]amino)-6-methylheptanoic acid 
• 854102-57-1 [(R)-3-methyl-1-phenethylbutyl]carbamic acid tert-butyl ester 

Relevant articles and documents

Synthesis of non-natural amino acids based on the ruthenium-catalysed oxidation of a phenyl group to carboxylic acid

An efficient method for the synthesis of enantiopure β-, β-, and δ-amino acids with proteinogenic side chains, starting from natural α-amino acids, was developed. The method is based on the ruthenium-catalyzed oxidation of a phenyl group to a carboxylic a