72119-96-1

Basic information

• Product Name: (Z)-2-aminocinnamonitrile
• CAS NO: 72119-96-1
• Molecular Weight: 144.176
• Mol File: 72119-96-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (Z)-2-aminocinnamonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-2-aminocinnamonitrile(72119-96-1)
• EPA Substance Registry System: (Z)-2-aminocinnamonitrile(72119-96-1)

Safety Data

• Hazardous Substances Data: 72119-96-1(Hazardous Substances Data)

Upstream product

• 123197-68-2 N-<2-(2-bromo-1-hydroxyethyl)phenyl>ethyl carbamate 
• 123197-70-6 2-ethoxycarbonylaminostyrene oxide 
• 122807-12-9 ethyl N-<2-(bromoacetyl)phenyl>carbamate 
• 6140-13-2 (2-acetylphenyl)carbamic acid ethyl ester 
• 552-89-6 2-nitro-benzaldehyde 
• 123197-72-8 N-<2-(2-cyano-1-hydroxyethyl)phenyl>ethyl carbamate 
• 74845-04-8 Z-1-cyano-2-(2'-nitrophenyl)ethene 

Downstream Products

• 86332-72-1 C₁₃H₁₂ClN₃O₂ 
• 74844-96-5 (Z)-3-(2-Azido-phenyl)-acrylonitrile 

Relevant articles and documents

BASIC MEDIA BEHAVIOR OF N- ETHYL CARBAMATES (Y=SMe, SOMe, SO2Me, H, Br, CN)

From the results obtained in the hydrolysis reaction of the carbamate group of some thioderivatives compounds whose common structure is (2-EtOOCNH-C6H4)-CHOH-CH2Y a mechanism is suggested to explain the products, as well as the relationship between the relative configuration of diastereoisomeric sulfoxides (Y=SOMe) with the reaction rate and with the stereochemical outcome.Other interesting and unexpected products are yielded when the hydrolysis reaction of other carbamates (Y=H, Br, CN) is carried out.In the present cases, the carbamate function seems to behave as a very versatile group capable of readily undergoing conversions to several kinds of heterocycles.