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Details

Stereochemistry ACHIRAL
Molecular Formula C6H7NO
Molecular Weight 109.1259
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYLHYDROXYLAMINE

SMILES

ONC1=CC=CC=C1

InChI

InChIKey=CKRZKMFTZCFYGB-UHFFFAOYSA-N
InChI=1S/C6H7NO/c8-7-6-4-2-1-3-5-6/h1-5,7-8H

HIDE SMILES / InChI

Molecular Formula C6H7NO
Molecular Weight 109.1259
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
N,O-diacyl-4-benzoyl-N-phenylhydroxylamines as photoinduced DNA cleaving agents.
2010-09-15
Clinical physiology and mechanism of dizocilpine (MK-801): electron transfer, radicals, redox metabolites and bioactivity.
2010-08-19
Eco-contribution for the production of N-arylnitrones: solvent-free and assisted by microwaves.
2010-06-22
Targeted LC-MS derivatization for aldehydes and carboxylic acids with a new derivatization agent 4-APEBA.
2010-05
Nitroreductase from Salmonella typhimurium: characterization and catalytic activity.
2010-04-21
Structural modifications of quinoline-based antimalarial agents: Recent developments.
2010-04
Water--more than just a green solvent: a stereoselective one-pot access to all-chiral tetrahydronaphthalenes in aqueous media.
2010-03-22
Structure-activity studies on arylamides and arysulfonamides Ras inhibitors.
2010-03
Monocyclic aromatic amines as potential human carcinogens: old is new again.
2010-01
Detection of endocrine disrupting chemicals in aerial invertebrates at sewage treatment works.
2009-12
Oriented organic islands and one-dimensional chains on a Au(111) surface fabricated by electrodeposition: an STM study.
2008-09-10
Application of the PM6 method to modeling the solid state.
2008-06
Transcriptome analysis of the response to chronic constant hypoxia in zebrafish hearts.
2008-01
Mechanistic studies of copper(I)-catalyzed allylic amination.
2007-12-12
An electrochemical and XPS study of reduction of nitrophenyl films covalently grafted to planar carbon surfaces.
2007-10-23
Silica-immobilized enzymes for multi-step synthesis in microfluidic devices.
2007-10-15
Electrochemical reduction of nitrobenzene at carbon nanotube electrode.
2007-09-05
Mechanistic study on aniline-induced erythrocyte toxicity.
2007-09
Synthesis of tetra-ortho-substituted, phosphorus-containing and carbonyl-containing biaryls utilizing a Diels-Alder approach.
2007-07-25
A phase I study of single administration of antibody-directed enzyme prodrug therapy with the recombinant anti-carcinoembryonic antigen antibody-enzyme fusion protein MFECP1 and a bis-iodo phenol mustard prodrug.
2006-11-01
Characterization of genes involved in the initial reactions of 4-chloronitrobenzene degradation in Pseudomonas putida ZWL73.
2006-11
Coimmobilization of a redox enzyme and a cofactor regeneration system.
2006-09-14
Microdroplet dissolution into a second-phase solvent using a micropipet technique: test of the Epstein-Plesset model for an aniline-water system.
2006-04-25
Double-layer effects and distance dependence of electron transfer in reduction of nitro aromatic radical anions.
2006-02-14
Genotoxic activities of aniline and its metabolites and their relationship to the carcinogenicity of aniline in the spleen of rats.
2005-12
Computational study on the mechanism and rate constant for the C6H5 + C6H5NO reaction.
2005-10-13
Design, synthesis and biological evaluation of sugar-derived Ras inhibitors.
2005-10
Substitution and condensation reactions with poly(anilineboronic acid): reactivity and characterization of thin films.
2005-04-12
Continuous synthesis of aminophenols from nitroaromatic compounds by combination of metal and biocatalyst.
2005-01-21
The hemotoxicity of para-substituted aniline analogs in dog and rat erythrocytes: a species comparison.
2005
Hemolytic potential of structurally related aniline halogenated hydroxylamines.
2005
Aniline derivative-induced methemoglobin in rats.
2005
Stepwise oxidation of anilines by cis-[RuIV(bpy)2(py)(O)]2+.
2004-08-23
Hapten-directed targeting to single-chain antibody receptors.
2004-05
The kinetics and mechanism of the ferrate(VI) oxidation of hydroxylamines.
2003-10-20
Interdependent chemical-electrochemical steps in retrometabolism-based drug and safer chemical design.
2002-02
Interaction between dioxoruthenium(VI) porphyrins and hydroxylamines: coordination of N-substituted hydroxylamine to ruthenium and X-ray crystal structures of ruthenium complexes with a unidentate nitrosoarene ligand.
2001-06-01
T cells ignore aniline, a prohapten, but respond to its reactive metabolites generated by phagocytes: possible implications for the pathogenesis of toxic oil syndrome.
2001-04
The inhibition of human cytomegalovirus (hCMV) protease by hydroxylamine derivatives.
1999-11-01
Purification and characterization of nitrobenzene nitroreductase from Pseudomonas pseudoalcaligenes JS45.
1995-07
Degradation of nitrobenzene by a Pseudomonas pseudoalcaligenes.
1993-08
Comparative nephrotoxicity of aspirin and phenacetin derivatives.
1971-11-27
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:52:56 GMT 2025
Edited
by admin
on Mon Mar 31 18:52:56 GMT 2025
Record UNII
282MU82Z9A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYLHYDROXYLAMINE
MI  
Systematic Name English
N-PHENYLHYDROXYLAMINE
HSDB  
Preferred Name English
N-PHENYLHYDROXYLAMINE [HSDB]
Common Name English
NCI-C60093
Code English
NSC-223099
Code English
PHENYLHYDROXYLAMINE, N-
Systematic Name English
PHENYLHYDROXYLAMINE [MI]
Common Name English
.BETA.-PHENYLHYDROXYLAMINE
Common Name English
N-HYDROXYANILINE
Systematic Name English
N-HYDROXYBENZENAMINE
Systematic Name English
Code System Code Type Description
HSDB
2884
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID3025889
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
FDA UNII
282MU82Z9A
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
MESH
C012484
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
WIKIPEDIA
PHENYLHYDROXYLAMINE
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
CAS
100-65-2
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
PUBCHEM
7518
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
MERCK INDEX
m8675
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY Merck Index
NSC
223099
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-875-6
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY
CHEBI
28902
Created by admin on Mon Mar 31 18:52:56 GMT 2025 , Edited by admin on Mon Mar 31 18:52:56 GMT 2025
PRIMARY