1610968-09-6

Basic information

• Product Name: benzyl N-[(8Z)-heptadec-8-en-1-yl]carbamate
• Synonyms: benzyl N-[(8Z)-heptadec-8-en-1-yl]carbamate
• CAS NO: 1610968-09-6
• Molecular Weight: 387.606
• Mol File: 1610968-09-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl N-[(8Z)-heptadec-8-en-1-yl]carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl N-[(8Z)-heptadec-8-en-1-yl]carbamate(1610968-09-6)
• EPA Substance Registry System: benzyl N-[(8Z)-heptadec-8-en-1-yl]carbamate(1610968-09-6)

Safety Data

• Hazardous Substances Data: 1610968-09-6(Hazardous Substances Data)

Upstream product

• 10335-69-0 Oleylhydroxamic acid 
• 100-51-6 benzyl alcohol 
• 112-62-9 Methyl oleate 
• 19788-74-0 cis-10-nonadecenoic acid methyl ester 
• 501-53-1 benzyl chloroformate 

Relevant articles and documents

A base-mediated self-propagative Lossen rearrangement of hydroxamic acids for the efficient and facile synthesis of aromatic and aliphatic primary amines

A variety of aromatic and aliphatic hydroxamic acids were converted to the corresponding primary amines via base-mediated rearrangement. This rearrangement could proceed with less than 1 equiv. of K2CO3 in polar solvents under thermal conditions with no external reagents. This rearrangement has several features including no external activating agents needed for promoting the rearrangement, less than one equivalent of a base is sufficient for the reaction, and a clean reaction in which only carbon dioxide is produced as a by-product. A self-propagating mechanism via an isocyanate intermediate is proposed and elementary reaction steps, namely, chain propagation reactions are supported by experiments.