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Details

Stereochemistry ACHIRAL
Molecular Formula C6H4N2O4
Molecular Weight 168.107
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-DINITROBENZENE

SMILES

[O-][N+](=O)C1=CC=C(C=C1)[N+]([O-])=O

InChI

InChIKey=FYFDQJRXFWGIBS-UHFFFAOYSA-N
InChI=1S/C6H4N2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H

HIDE SMILES / InChI

Molecular Formula C6H4N2O4
Molecular Weight 168.107
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Metal binding characteristics of a laterally nonsymmetric aza cryptand upon functionalization with a pi-acceptor group.
2003 Aug 11
Alkylation of nitroaromatics with trialkyborane.
2003 May 30
Immunotherapy of basal cell carcinoma: evolving approaches.
2003 Oct
Thermally-treated clay as a stationary phase in liquid chromatography.
2004 Jul 9
Molecular optical gating devices based on polymer nanosheets assemblies.
2004 Mar 31
Sertoli cell junctional proteins as early targets for different classes of reproductive toxicants.
2004 May
PABA/NO as an anticancer lead: analogue synthesis, structure revision, solution chemistry, reactivity toward glutathione, and in vitro activity.
2006 Feb 9
Interactions of nitroaromatic compounds with the mammalian selenoprotein thioredoxin reductase and the relation to induction of apoptosis in human cancer cells.
2006 Mar 3
Transport mechanisms for the uptake of organic compounds by rice (Oryza sativa) roots.
2007 Jul
Discrimination of nitroaromatics and explosives mimics by a fluorescent Zn(salicylaldimine) sensor array.
2008 Apr 23
1-[2-(2,4-Dinitro-benzyl-ideneamino)phen-yl]-3-phenyl-thio-urea.
2009 Sep 12
Metastable anions of dinitrobenzene: resonances for electron attachment and kinetic energy release.
2010 Dec 28
Toxicant-induced leakage of germ cell-specific proteins from seminiferous tubules in the rat: relationship to blood-testis barrier integrity and prospects for biomonitoring.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:39:38 GMT 2025
Edited
by admin
on Mon Mar 31 19:39:38 GMT 2025
Record UNII
784Q9O56S9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,4-DINITROBENZENE
HSDB  
Preferred Name English
P-DINITROBENZENE
MI  
Common Name English
P-DINITROBENZENE [MI]
Common Name English
NSC-3809
Code English
BENZENE, P-DINITRO-
Common Name English
1,4-DINITROBENZENE [HSDB]
Common Name English
BENZENE, 1,4-DINITRO-
Systematic Name English
DINITROBENZENE, P-
Common Name English
PARA-DINITROBENZENE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
1,4-Dinitrobenzene
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
MESH
C053052
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
PUBCHEM
7492
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
NSC
3809
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
CAS
100-25-4
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
HSDB
4485
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID0021836
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
MERCK INDEX
m4569
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
202-833-7
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
CHEBI
51398
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY
FDA UNII
784Q9O56S9
Created by admin on Mon Mar 31 19:39:38 GMT 2025 , Edited by admin on Mon Mar 31 19:39:38 GMT 2025
PRIMARY