1823-91-2,MFCD00001871
Catalog No.:AA0023JJ

1823-91-2 | Alpha-methylphenylacetonitrile

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
96%
in stock  
$28.00   $19.00
- +
1g
96%
in stock  
$29.00   $20.00
- +
5g
96%
in stock  
$46.00   $32.00
- +
25g
96%
in stock  
$140.00   $98.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0023JJ
Chemical Name:
Alpha-methylphenylacetonitrile
CAS Number:
1823-91-2
Molecular Formula:
C9H9N
Molecular Weight:
131.1745
MDL Number:
MFCD00001871
SMILES:
CC(c1ccccc1)C#N
Properties
Properties
 
BP:
231 °C  
Form:
Liquid  
Refractive Index:
n20/D 1.5106(lit.)  

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

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

Journal: Organic & biomolecular chemistry 20110421

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

Journal: BMC biotechnology 20110101

Title: Lewis acid controlled regioselectivity in styrene hydrocyanation.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20090907

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

Journal: Chemical communications (Cambridge, England) 20090714

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

Journal: Applied microbiology and biotechnology 20081101

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

Journal: Studies in mycology 20080101

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

Journal: Protein engineering, design & selection : PEDS 20070801

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

Journal: The Journal of organic chemistry 20050610

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

Journal: The Journal of organic chemistry 20020222

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

Journal: Biotechnology and applied biochemistry 20020201

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SDS
Tags:1823-91-2 Molecular Formula|1823-91-2 MDL|1823-91-2 SMILES|1823-91-2 Alpha-methylphenylacetonitrile
Catalog No.: AA0023JJ
1823-91-2,MFCD00001871
1823-91-2 | Alpha-methylphenylacetonitrile
Pack Size: 250mg
Purity: 96%
in stock
$28.00 $19.00
Pack Size: 1g
Purity: 96%
in stock
$29.00 $20.00
Pack Size: 5g
Purity: 96%
in stock
$46.00 $32.00
Pack Size: 25g
Purity: 96%
in stock
$140.00 $98.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA0023JJ
Chemical Name: Alpha-methylphenylacetonitrile
CAS Number: 1823-91-2
Molecular Formula: C9H9N
Molecular Weight: 131.1745
MDL Number: MFCD00001871
SMILES: CC(c1ccccc1)C#N
Properties
BP: 231 °C  
Form: Liquid  
Refractive Index: n20/D 1.5106(lit.)  
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 fold

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

Journal: Organic & biomolecular chemistry20110421

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

Journal: BMC biotechnology20110101

Title: Lewis acid controlled regioselectivity in styrene hydrocyanation.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20090907

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

Journal: Chemical communications (Cambridge, England)20090714

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

Journal: Applied microbiology and biotechnology20081101

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

Journal: Studies in mycology20080101

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

Journal: Protein engineering, design & selection : PEDS20070801

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

Journal: The Journal of organic chemistry20050610

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

Journal: The Journal of organic chemistry20020222

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

Journal: Biotechnology and applied biochemistry20020201

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