100038-71-9

Basic information

• Product Name: (E)-2-Benzyloxycarbonylamino-non-3-enoic acid methyl ester
• CAS NO: 100038-71-9
• Molecular Weight: 319.401
• Mol File: 100038-71-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-2-Benzyloxycarbonylamino-non-3-enoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-Benzyloxycarbonylamino-non-3-enoic acid methyl ester(100038-71-9)
• EPA Substance Registry System: (E)-2-Benzyloxycarbonylamino-non-3-enoic acid methyl ester(100038-71-9)

Safety Data

• Hazardous Substances Data: 100038-71-9(Hazardous Substances Data)

Upstream product

• 61759-16-8 (2-Phenylseleno)heptanal 
• 14952-06-8 methyl (2E)-2-nonenoate 
• 621-84-1 O-benzyl carbamate 
• 100038-64-0 methyl 4-(phenylseleno)-2(E)-nonenoate 

Relevant articles and documents

Allylic Selenides in Organic Synthesis: New Methods for the Synthesis of Allylic Amines

Oxidative rearrangement of allylic selenides in the presence of various amine nucleophiles provides synthetic access to a variety of allylic amine derivatives.The stereochemical outcome of these reactions has been investigated, and is consistent with a -sigmatropic rearrangement mechanism.Several D-α-amino acids and racemic β,γ-unsaturated α-amino acids were prepared in this manner.A variant of this process employing an achiral allylic selenide and chiral amide afforded protected allylic amines in low diastereoisomeric excess.