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Details

Stereochemistry ACHIRAL
Molecular Formula C12H9NO2
Molecular Weight 199.2054
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-NITROBIPHENYL

SMILES

[O-][N+](=O)C1=CC=CC=C1C2=CC=CC=C2

InChI

InChIKey=YOJKKXRJMXIKSR-UHFFFAOYSA-N
InChI=1S/C12H9NO2/c14-13(15)12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H

HIDE SMILES / InChI

Molecular Formula C12H9NO2
Molecular Weight 199.2054
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screening.
2009-07-23
Molecular electronics using diazonium-derived adlayers on carbon with Cu top contacts: critical analysis of metal oxides and filaments.
2008-09-17
Poly(2,7-carbazole)s: structure-property relationships.
2008-09
1,1,1,3,3,3-Hexafluoro-2,2-bis-[4-(4-nitro-phen-oxy)phen-yl]propane.
2008-07-19
Ultraviolet-visible spectroelectrochemistry of chemisorbed molecular layers on optically transparent carbon electrodes.
2007-11
Electron transport and redox reactions in carbon-based molecular electronic junctions.
2006-06-14
Determination of the structure and orientation of organic molecules tethered to flat graphitic carbon by ATR-FT-IR and Raman spectroscopy.
2006-05-01
Beta-cyclodextrin and its derivatives-enhanced solubility and biodegradation of 2-nitrobiphenyl.
2006
Triphenylphosphine-mediated reductive cyclization of 2-nitrobiphenyls: a practical and convenient synthesis of carbazoles.
2005-06-24
Strong effects of molecular structure on electron transport in carbon/molecule/copper electronic junctions.
2005-06-09
Substituent effects on the oxidation of substituted biphenyl congeners by type II methanotroph strain CSC1.
2005-05
Detection of nitrated benzene metabolites in bone marrow of B6C3F1 mice treated with benzene.
2004-03
[Isomeric phenanthridines from 1,2-dihydro-5-methyl-2'-nitro-[1,1'-biphenyl]-2,6-dicarboxylic acid esters].
2003-11
Mono- and multilayer formation by diazonium reduction on carbon surfaces monitored with atomic force microscopy "scratching".
2003-08-01
Modified carbon surfaces as "organic electrodes" that exhibit conductance switching.
2003-01-15
Enhanced photoreactivity of the nitrobiphenyl chromophore.
2002-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:07:32 GMT 2025
Edited
by admin
on Mon Mar 31 21:07:32 GMT 2025
Record UNII
8R1N47E4DT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-5532
Preferred Name English
O-NITROBIPHENYL
MI  
Common Name English
2'-NITROBIPHENYL
Systematic Name English
BIPHENYL, 2-NITRO-
Systematic Name English
1,1'-BIPHENYL, 2-NITRO-
Systematic Name English
2-NITRO-1,1'-BIPHENYL
Systematic Name English
ONB
Common Name English
2-PHENYLNITROBENZENE
Systematic Name English
O-NITROBIPHENYL [MI]
Common Name English
2-NITROBIPHENYL
Systematic Name English
Code System Code Type Description
NSC
5532
Created by admin on Mon Mar 31 21:07:32 GMT 2025 , Edited by admin on Mon Mar 31 21:07:32 GMT 2025
PRIMARY
PUBCHEM
6829
Created by admin on Mon Mar 31 21:07:32 GMT 2025 , Edited by admin on Mon Mar 31 21:07:32 GMT 2025
PRIMARY
CAS
86-00-0
Created by admin on Mon Mar 31 21:07:32 GMT 2025 , Edited by admin on Mon Mar 31 21:07:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID9025746
Created by admin on Mon Mar 31 21:07:32 GMT 2025 , Edited by admin on Mon Mar 31 21:07:32 GMT 2025
PRIMARY
MERCK INDEX
m7949
Created by admin on Mon Mar 31 21:07:32 GMT 2025 , Edited by admin on Mon Mar 31 21:07:32 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
201-646-8
Created by admin on Mon Mar 31 21:07:32 GMT 2025 , Edited by admin on Mon Mar 31 21:07:32 GMT 2025
PRIMARY
FDA UNII
8R1N47E4DT
Created by admin on Mon Mar 31 21:07:32 GMT 2025 , Edited by admin on Mon Mar 31 21:07:32 GMT 2025
PRIMARY