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1795-83-1 | Acetamide, N-hydroxy-N-phenyl-
CAS No: 1795-83-1 Catalog No: AG00271R MDL No:
Product Description
Catalog Number:
AG00271R
Chemical Name:
Acetamide, N-hydroxy-N-phenyl-
CAS Number:
1795-83-1
Molecular Formula:
C8H9NO2
Molecular Weight:
151.1626
IUPAC Name:
N-hydroxy-N-phenylacetamide
InChI:
InChI=1S/C8H9NO2/c1-7(10)9(11)8-5-3-2-4-6-8/h2-6,11H,1H3
InChI Key:
GMJUGPZVHVVVCG-UHFFFAOYSA-N
SMILES:
ON(c1ccccc1)C(=O)C
Properties
Complexity:
141
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
151.063g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
151.165g/mol
Monoisotopic Mass:
151.063g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.8
Literature
| Title | Journal |
|---|---|
| Intensification of biocatalytical processes by synergistic substrate conversion. Fungal peroxidase catalyzed N-hydroxy derivative oxidation in presence of 10-propyl sulfonic acid phenoxazine. | Applied biochemistry and biotechnology 20090801 |
| Engineering and Applications of fungal laccases for organic synthesis. | Microbial cell factories 20080101 |
| Enzymatic and mechanistic studies on the formation of N-phenylglycolohydroxamic acid from nitrosobenzene and pyruvate in spinach leaf homogenate. | Journal of agricultural and food chemistry 20060125 |
| Role of oxidative enzymatic treatments on enzymatic hydrolysis of softwood. | Biotechnology and bioengineering 20040605 |
| Investigation of hydroxamic acids as laccase-mediators for pulp bleaching. | Applied microbiology and biotechnology 20040501 |
| Hydrogen bonding between histidine and lignin model compounds or redox mediators as calculated with the DFT method. Effects on the ease of oxidation. | Organic & biomolecular chemistry 20040221 |
| Enzymatic and electrochemical oxidation of N-hydroxy compounds. Redox potential, electron-transfer kinetics, and radical stability. | European journal of biochemistry 20010801 |
| Structure-activity relationships in the deacetylation of O-glucosides of N-hydroxy-N-arylacylamides by mammalian liver microsomes. | Chemico-biological interactions 20010731 |
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