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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
Enhanced photoreactivity of the nitrobiphenyl chromophore.
2002 Jan
Mono- and multilayer formation by diazonium reduction on carbon surfaces monitored with atomic force microscopy "scratching".
2003 Aug 1
[Isomeric phenanthridines from 1,2-dihydro-5-methyl-2'-nitro-[1,1'-biphenyl]-2,6-dicarboxylic acid esters].
2003 Nov
Detection of nitrated benzene metabolites in bone marrow of B6C3F1 mice treated with benzene.
2004 Mar
Triphenylphosphine-mediated reductive cyclization of 2-nitrobiphenyls: a practical and convenient synthesis of carbazoles.
2005 Jun 24
Strong effects of molecular structure on electron transport in carbon/molecule/copper electronic junctions.
2005 Jun 9
Substituent effects on the oxidation of substituted biphenyl congeners by type II methanotroph strain CSC1.
2005 May
Determination of the structure and orientation of organic molecules tethered to flat graphitic carbon by ATR-FT-IR and Raman spectroscopy.
2006 May 1
Ultraviolet-visible spectroelectrochemistry of chemisorbed molecular layers on optically transparent carbon electrodes.
2007 Nov
1,1,1,3,3,3-Hexafluoro-2,2-bis-[4-(4-nitro-phen-oxy)phen-yl]propane.
2008 Jul 19
Poly(2,7-carbazole)s: structure-property relationships.
2008 Sep
Molecular electronics using diazonium-derived adlayers on carbon with Cu top contacts: critical analysis of metal oxides and filaments.
2008 Sep 17
One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screening.
2009 Jul 23
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:03:26 GMT 2023
Edited
by admin
on Sat Dec 16 02:03:26 GMT 2023
Record UNII
8R1N47E4DT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
O-NITROBIPHENYL
MI  
Common Name English
NSC-5532
Code 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 Sat Dec 16 02:03:26 GMT 2023 , Edited by admin on Sat Dec 16 02:03:26 GMT 2023
PRIMARY
PUBCHEM
6829
Created by admin on Sat Dec 16 02:03:26 GMT 2023 , Edited by admin on Sat Dec 16 02:03:26 GMT 2023
PRIMARY
CAS
86-00-0
Created by admin on Sat Dec 16 02:03:26 GMT 2023 , Edited by admin on Sat Dec 16 02:03:26 GMT 2023
PRIMARY
EPA CompTox
DTXSID9025746
Created by admin on Sat Dec 16 02:03:26 GMT 2023 , Edited by admin on Sat Dec 16 02:03:26 GMT 2023
PRIMARY
MERCK INDEX
m7949
Created by admin on Sat Dec 16 02:03:26 GMT 2023 , Edited by admin on Sat Dec 16 02:03:26 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
201-646-8
Created by admin on Sat Dec 16 02:03:26 GMT 2023 , Edited by admin on Sat Dec 16 02:03:26 GMT 2023
PRIMARY
FDA UNII
8R1N47E4DT
Created by admin on Sat Dec 16 02:03:26 GMT 2023 , Edited by admin on Sat Dec 16 02:03:26 GMT 2023
PRIMARY