1823-91-2 | Alpha-methylphenylacetonitrile

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$15.00	$10.00
1g	96%	in stock	$16.00	$11.00
5g	96%	in stock	$33.00	$23.00
25g	96%	in stock	$133.00	$93.00

Description

• Catalog Number: AA97803
• Chemical Name: Alpha-methylphenylacetonitrile
• CAS Number: 1823-91-2
• Molecular Formula: C9H9N
• Molecular Weight: 131.17446
• MDL Number: MFCD00001871
• SMILES: CC(c1ccccc1)C#N

Computed Properties

• Complexity: 136
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 2.1

Literature

• Probing the enantioselectivity of a diverse group of purified cobalt-centred nitrile hydratases.

  Organic & biomolecular chemistry 20110421

• Heterologous expression, purification and characterization of nitrilase from Aspergillus niger K10.

  BMC biotechnology 20110101

• Lewis acid controlled regioselectivity in styrene hydrocyanation.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090907

• Nickel/AlMe(2)Cl-catalysed carbocyanation of alkynes using arylacetonitriles.

  Chemical communications (Cambridge, England) 20090714

• Utilization of arylaliphatic nitriles by haloalkaliphilic Halomonas nitrilicus sp. nov. isolated from soda soils.

  Applied microbiology and biotechnology 20081101

• Characterisation of the substrate specificity of the nitrile hydrolyzing system of the acidotolerant black yeast Exophiala oligosperma R1.

  Studies in mycology 20080101

• Influence of different carboxy-terminal mutations on the substrate-, reaction- and enantiospecificity of the arylacetonitrilase from Pseudomonas fluorescens EBC191.

  Protein engineering, design & selection : PEDS 20070801

• Kinetics of the reaction between 2-phenylpropionitrile and 2-chloro-5-nitrotrifluoromethylbenzene under phase-transfer catalysis.

  The Journal of organic chemistry 20050610

• Selective mono-C-methylations of arylacetonitriles and arylacetates with dimethylcarbonate: a mechanistic investigation.

  The Journal of organic chemistry 20020222

• Enhancement of enzyme activity and enantioselectivity via cultivation in nitrile metabolism by Rhodococcus sp. CGMCC 0497.

  Biotechnology and applied biochemistry 20020201