132741-32-3

Basic information

• Product Name: Benzeneacetonitrile, 3,5-difluoro-a-hydroxy-
• Synonyms: Benzeneacetonitrile, 3,5-difluoro-a-hydroxy-;2-(3,5-difluorophenyl)-2-hydroxyacetonitrile
• CAS NO: 132741-32-3
• Molecular Formula: C8H5F2NO
• Molecular Weight: 169.1282064
• Mol File: 132741-32-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 268.5°C at 760 mmHg
• Flash Point: 116.2°C
• Appearance: /
• Density: 1.382g/cm³
• Vapor Pressure: 0.00379mmHg at 25°C
• Refractive Index: 1.52
• PKA: 9.89±0.20(Predicted)
• CAS DataBase Reference: Benzeneacetonitrile, 3,5-difluoro-a-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetonitrile, 3,5-difluoro-a-hydroxy-(132741-32-3)
• EPA Substance Registry System: Benzeneacetonitrile, 3,5-difluoro-a-hydroxy-(132741-32-3)

Safety Data

• Hazardous Substances Data: 132741-32-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H5F2NO/c9-6-1-5(8(12)4-11)2-7(10)3-6/h1-3,8,12H

Upstream product

• 32085-88-4 3,5-difluorobenzaldehyde 
• 143-33-9 sodium cyanide 
• 773837-37-9 sodium cyanide 

Downstream Products

• 1584127-59-2 methyl 2-acetoxy-2-(3,5-difluorophenyl)acetate 
• 208259-37-4 methyl 2-(3,5-difluorophenyl)-2-hydroxyacetate 
• 1584127-72-9 C₉H₈F₂O₃ 
• 1584127-69-4 (S)-(+)-methyl 2-acetoxy-2-(3,5-difluorophenyl)acetate 

Relevant articles and documents

Kinetic resolution of mandelate esters via stereoselective acylation catalyzed by lipase PS-30

By using lipase PS-30 as catalyst, the kinetic resolution of a series of racemic mandelate esters has been achieved via stereoselective acylation. The value of kinetic enantiomeric ratio (E) reached up to 197.5. Substituent effect is briefly discussed.

4-ethyl-3-(substituted phenyl)-1-(3-trifluoromethylphenyl)-2-pyrrolidinone derivatives, herbicidal compositions containing them and use thereof

4-Ethyl-3-(phenyl)-1-(3-trifluoromethylphenyl)-2-pyrrolidinones and corresponding compounds bearing a p-substituent on the 1-position phenyl group and/or a substituent on the 3-position phenyl group exhibit selective herbicidal activities against various