Home Nitro Compounds 6388-74-5
6388-74-5,MFCD00181340
Catalog No.:AA00IB7R

6388-74-5 | 2-(4-Nitrophenyl)oxirane

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$74.00   $52.00
- +
250mg
95%
in stock  
$121.00   $85.00
- +
1g
95%
in stock  
$308.00   $216.00
- +
5g
95%
in stock  
$984.00   $689.00
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  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00IB7R
Chemical Name:
2-(4-Nitrophenyl)oxirane
CAS Number:
6388-74-5
Molecular Formula:
C8H7NO3
Molecular Weight:
165.1461
MDL Number:
MFCD00181340
SMILES:
[O-][N+](=O)c1ccc(cc1)C1OC1
NSC Number:
72312
Properties
Properties
 
Storage:
2-8℃;Inert atmosphere;  

Computed Properties
 
Complexity:
181  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
1.2  

Literature

Title: Reactivity of p-nitrostyrene oxide as an alkylating agent. A kinetic approach to biomimetic conditions.

Journal: Organic & biomolecular chemistry 20111021

Title: Influence of pH on the expression of a recombinant epoxide hydrolase in Aspergillus niger.

Journal: Biotechnology journal 20090501

Title: Production of epoxide hydrolases in batch fermentations of Botryosphaeria rhodina.

Journal: Journal of industrial microbiology & biotechnology 20080601

Title: Inactivation of epoxide hydrolase by catalysis-induced formation of isoaspartate.

Journal: FEBS letters 20080514

Title: Cloning, expression, purification, and characterization of a novel epoxide hydrolase from Aspergillus niger SQ-6.

Journal: Protein expression and purification 20070601

Title: Enantioconvergent hydrolysis of styrene epoxides by newly discovered epoxide hydrolases in mung bean.

Journal: Organic letters 20060413

Title: Purification and characterisation of a novel enantioselective epoxide hydrolase from Aspergillus niger M200.

Journal: Biochimica et biophysica acta 20060201

Title: Structural basis for the enantioselectivity of an epoxide ring opening reaction catalyzed by halo alcohol dehalogenase HheC.

Journal: Journal of the American Chemical Society 20050928

Title: Kinetic mechanism and enantioselectivity of halohydrin dehalogenase from Agrobacterium radiobacter.

Journal: Biochemistry 20030513

Title: Biocatalysis of nitro substituted styrene oxides by non-conventional yeasts.

Journal: Biotechnology letters 20030501

Title: A spectrophotometric method to assay epoxide hydrolase activity.

Journal: Journal of biochemical and biophysical methods 20011204

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