5841-70-3

Basic information

• Product Name: 2-CYANO-2-PHENYLVINYLALCOHOL
• Synonyms: 3-HYDROXY-2-PHENYLACRYLONITRILE;2-CYANO-2-PHENYLVINYLALCOHOL;2-CYANO-2-PHENYLACETALDEHYDE;3-Oxo-2-phenylpropionitrile;sodium (Z)-2-cyano-2-phenylethylenolate
• CAS NO: 5841-70-3
• Molecular Formula: C₉H₇NO
• Molecular Weight: 145.16
• Product Categories: Benzene series
• Mol File: 5841-70-3.mol
• Article Data: 15

Chemical Properties

• Melting Point: 157-160°C
• Boiling Point: 242.7 ºC at 760 mmHg
• Flash Point: 100.6 ºC
• Appearance: /
• Density: 1.114 g/cm³
• Vapor Pressure: 0.0335mmHg at 25°C
• Refractive Index: 1.535
• CAS DataBase Reference: 2-CYANO-2-PHENYLVINYLALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CYANO-2-PHENYLVINYLALCOHOL(5841-70-3)
• EPA Substance Registry System: 2-CYANO-2-PHENYLVINYLALCOHOL(5841-70-3)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: 3439
• Hazardous Substances Data: 5841-70-3(Hazardous Substances Data)

Usage

General Description

2-Cyano-2-phenylvinylalcohol, also known as 2-(2-Hydroxyethenyl)-benzonitrile or 2-Phenyl-2-cyanovinyl alcohol, is a chemical compound often used in the field of organic chemistry. Its molecular formula is C9H7NO, and it has a molar mass of 145.16 g/mol. 2-Cyano-2-phenylvinylalcohol may exist as a clear, colorless liquid or as a white crystal solid and has relatively moderate stability under normal conditions of handling and storage. Primary hazards while handling 2-Cyano-2-phenylvinylalcohol are risks of irritation to eyes, skin or respiratory systems due to its potentially corrosive nature. It is not classified as a hazardous substance in any known regulatory listing, but standard precautionary measures should be taken while handling.

InChI:InChI=1/C9H7NO/c10-6-9(7-11)8-4-2-1-3-5-8/h1-5,7,9H

Upstream product

• 60-29-7 diethyl ether 
• 26388-11-4 Natrium-phenylacetonitril 
• 109-94-4 formic acid ethyl ester 
• 140-29-4 phenylacetonitrile 
• 68-12-2 N,N-dimethyl-formamide 
• 73591-12-5 3-benzoyloxy-2-phenyl-acrylonitrile 
• 31881-80-8 (Z)-2-phenyl-3-(p-tolylamino)acrylonitrile 
• 57488-21-8 (Z)-2-phenyl-3-(piperidin-1-yl)acrylonitrile 
• 1823-91-2 1-phenylethyl cyanide 
• 141-52-6 sodium ethanolate 

Downstream Products

• 22211-28-5 methyl ether of the enol of α-formyl-α-phenylacetonitrile 
• 18588-49-3 2,4-diamino-5-phenyl pyrimidine 
• 22156-56-5 2-phenyl-3-propoxy-acrylonitrile 
• 2555-22-8 3-phenyl-7-methoxycoumarin 
• 6468-93-5 5,7-dihydroxy-3-phenylcoumarin 
• 36122-35-7 2-phenylmaleic anhydride 
• 20759-62-0 6,7-dihydroxy-3-phenyl-2H-chromen-2-one 
• 22156-55-4 3-ethoxy-2-phenylacrylonitrile 
• 91392-86-8 (2Ξ,4R)-2-((Ξ)-cyano-phenyl-methyl)-thiazolidine-4-carboxylic acid 
• 582-22-9 2-phenylpropylamine 
• 98398-22-2 bis(2-phenylpropyl)amine 
• 22156-60-1 2,2'-diphenyl-3,3'-imino-di-acrylonitrile 
• 32016-25-4 7-amino-3,6-diphenylpyrazolo<1,5-a>pyrimidine 
• 88456-37-5 3,3-diethoxy-2-phenyl-propionitrile 

Relevant articles and documents

Preparation and application of novel quinolizine pH fluorescence molecular probe

The invention discloses a novel quinolizine pH fluorescence molecular probe which has brand-new action mechanism as shown in the specification, wherein a skeleton structure is 4H-quinolizine-4-imine as shown in the compound in the formula II, C-N bond in

COMPOUNDS AND MATRICES FOR USE IN BONE GROWTH AND REPAIR

Compositions of small molecules, matrices, and isolated cells including methods of preparation, and methods for differentiation, transdifferentiation, and proliferation of animal cells into the osteoblast blast cell lineage were described. Examples of ost

Copper-catalyzed N-aryl-β-enaminonitrile synthesis utilizing isocyanides as the nitrogen source

A novel synthetic protocol for N-aryl-β-enaminonitriles, which are useful building blocks for heterocycle synthesis, was developed using isocyanides as the nitrogen source. Using copper-catalyzed one-step reactions between isocyanides and benzyl cyanides under mild conditions, diverse N-aryl-β-enaminonitriles could be synthesized in excellent yields and with high atom-efficiency. N-Alkyl-β-enaminonitriles were also synthesized in good yields. A mechanism involving an imidoyl-copper intermediate was proposed based on mechanistic studies and previous reports. In addition, we demonstrated that a synthesized N-aryl-β-enaminonitrile could be utilized for the synthesis of a β-keto nitrile compound and 3-aminopyrazole.