485759-27-1

Basic information

• Product Name: Benzeneacetonitrile, 2-fluoro-alpha-hydroxy-, (alphaS)- (9CI)
• Synonyms: Benzeneacetonitrile, 2-fluoro-alpha-hydroxy-, (alphaS)- (9CI)
• CAS NO: 485759-27-1
• Molecular Formula: C8H6FNO
• Molecular Weight: 151.1377432
• Product Categories: HALIDE
• Mol File: 485759-27-1.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzeneacetonitrile, 2-fluoro-alpha-hydroxy-, (alphaS)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetonitrile, 2-fluoro-alpha-hydroxy-, (alphaS)- (9CI)(485759-27-1)
• EPA Substance Registry System: Benzeneacetonitrile, 2-fluoro-alpha-hydroxy-, (alphaS)- (9CI)(485759-27-1)

Safety Data

• Hazardous Substances Data: 485759-27-1(Hazardous Substances Data)

Upstream product

• 151-50-8 potassium cyanide 
• 446-52-6 2-Fluorobenzaldehyde 
• 74-90-8 hydrogen cyanide 
• 108-05-4 vinyl acetate 
• 133721-88-7 (+/-)-2-hydroxy-2-(2-fluorophenyl)acetonitrile 
• 1070980-35-6 (R)-2-(2-fluorophenyl)-2-(trimethylsilyloxy)acetonitrile 
• 82128-76-5 α-[(trimethylsilyl)oxy]-α-(o-fluorophenyl)acetonitrile 
• 773837-37-9 sodium cyanide 
• 7677-24-9 trimethylsilyl cyanide 

Downstream Products

• 192884-55-2 methyl 2-(2-fluorophenyl)-2-hydroxyacetate 
• 1584127-58-1 C₁₁H₁₁FO₄ 
• 175134-34-6 (S)-2-(2-fluorophenyl)-2-hydroxyacetic acid 

Relevant articles and documents

Enantioselective cyanosilylation of aldehydes catalyzed by a multistereogenic salen-Mn(III) complex with a rotatable benzylic group as a helping hand

A multistereogenic salen-Mn(iii) complex bearing an aromatic pocket and two benzylic groups as helping hands was found to be efficient in the catalysis of asymmetric cyanosilylation. The salen-Mn catalyst partially mimics the functions of biocatalysts by

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.

Enantioselective cyanosilylation of aldehydes catalyzed by novel camphor derived Schiff bases-titanium(IV) complexes

Five tridentate Schiff bases have been prepared from (1R,2S,3R,4S)-3-amino- 1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol and salicylaldehydes. X-ray structure investigation revealed differences in their molecular conformation, and their titanium(IV) complexes