56069-64-8

Basic information

• Product Name: 2-Propenenitrile, 2-formyl-3-phenyl-
• CAS NO: 56069-64-8
• Molecular Formula: C10H7NO
• Molecular Weight: 157.172
• Mol File: 56069-64-8.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: 2-Propenenitrile, 2-formyl-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenenitrile, 2-formyl-3-phenyl-(56069-64-8)
• EPA Substance Registry System: 2-Propenenitrile, 2-formyl-3-phenyl-(56069-64-8)

Safety Data

• Hazardous Substances Data: 56069-64-8(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 2700-22-3 Benzylidenemalononitrile 
• 57597-62-3 3,3-dimethoxypropionitrile 
• 99686-39-2 (E)-2-bromo-3-phenylprop-2-enal 
• 75-86-5 2-hydroxy-2-methylpropanenitrile 
• 645-59-0 dihydrocinnamonitrile 
• 497088-75-2 2-benzyl-3-oxopropanenitrile 
• 1247933-44-3 (E)-2-(diethoxymethyl)-3-phenylacrylonitrile 
• 107-13-1 acrylonitrile 
• 2032-34-0 3,3-bis(ethyloxy)propanenitrile 
• 139413-81-3 (E)-2-(bromomethyl)-3-phenylacrylonitrile 
• 75-65-0 tert-butyl alcohol 
• 131202-39-6 [2E]-2-Cyano-3-phenylprop-2-enol 
• 163921-40-2 (E)-2-Dimethoxymethyl-3-phenyl-acrylonitrile 

Downstream Products

• 497088-75-2 2-benzyl-3-oxopropanenitrile 
• 214540-68-8 4-Methyl-benzenesulfinic acid [(Z)-2-cyano-3-phenyl-prop-2-en-(E)-ylidene]-amide 
• 146385-89-9 methyl 3-amino-4-benzyl-1H-pyrrole-2-carboxylate 
• 1392817-33-2 7-benzyl-4-chloro-2-methyl-5H-pyrrolo[3,2-d]pyrimidine 
• 348637-56-9 1-methyl-4-phenyl-1H-pyrrole-3-carbonitrile 
• 709-79-5 (E)-2-cyano-3-phenylacrylamide 
• 192653-52-4 methyl 3-({[(methoxycarbonyl)amino][(methoxycarbonyl)imino]methyl}amino)-4-(phenylmethyl)-1H-pyrrole-2-carboxylate 
• 197850-25-2 (7-Benzyl-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-2-yl)-carbamic acid methyl ester 
• 132138-67-1 2-Amino-3,5-dihydro-7-(phenylmethyl)-4H-pyrrolo[3,2-d]pyrimidin-4-one 

Relevant articles and documents

A facile synthesis of [E]-α-cyanocinnamic aldehydes from Baylis-Hillman adducts

A facile synthesis of stereochemically pure [E]-α-cyanocinnamic aldehydes from Baylis-Hillman adducts is described.

An efficient catalyst-free one-pot synthesis of primary amides from the aldehydes of the Baylis-Hillman reaction

Herein, a facile and efficient method for the preparation of allyl amides from the aldehyde of Baylis-Hillman adducts has been developed using a hydroxylamine/methanol system under a catalyst-free condition. The effects of solvents and temperature on the reaction and substituents on the phenyl ring have been examined. This method is best demonstrated by its advantages such as operational simplicity, moderate to excellent yields, short reaction time, and simple reaction procedure. Most importantly, the reaction proceeds smoothly in the absence of a catalyst and an external oxidant.

Hypervalent iodine catalysis for selective oxidation of Baylis-Hillman adducts via in situ generation of o-iodoxybenzoic acid (IBX) from 2-iodosobenzoic acid (IBA) in the presence of oxone

An efficient, environmentally benign, eco-friendly protocol for selective oxidation of primary and secondary Baylis-Hillman alcohols to the corresponding carbonyl compounds has been developed. We have demonstrated the catalytic use of o-iodoxybenzoic acid