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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
Metastable anions of dinitrobenzene: resonances for electron attachment and kinetic energy release.
2010-12-28
Fluorescent polymer sensor array for detection and discrimination of explosives in water.
2010-12-01
Toxicant-induced leakage of germ cell-specific proteins from seminiferous tubules in the rat: relationship to blood-testis barrier integrity and prospects for biomonitoring.
2010-10
Impact of enteral nutrition on nitrogen balance in patients of trauma.
2010-04
[An acute dinitrobenzene poisoning accident].
2010-03
Steroid assays in paediatric endocrinology.
2010
Triethyl-ammonium 2,4-dinitro-phenyl-barbiturate.
2009-09-26
1-[2-(2,4-Dinitro-benzyl-ideneamino)phen-yl]-3-phenyl-thio-urea.
2009-09-12
Efficacy of intracolonic administration of low-molecular-weight heparin CB-01-05, compared to other low-molecular-weight heparins and unfractionated heparin, in experimentally induced colitis in rat.
2008-12
A single molecule rectifier with strong push-pull coupling.
2008-11-28
2,4-Dichloro-benzaldehyde 2,4-dinitro-phenyl-hydrazone.
2008-07-09
Temperature tunability of size in CdS nanoparticles and size dependent photocatalytic degradation of nitroaromatics.
2008-06-01
Discrimination of nitroaromatics and explosives mimics by a fluorescent Zn(salicylaldimine) sensor array.
2008-04-23
Vascularization of the dorsal root ganglia and peripheral nerve of the mouse: implications for chemical-induced peripheral sensory neuropathies.
2008-03-19
Metastable dissociation of anions formed by electron attachment.
2008-03-14
Imaging of EGFR and EGFR tyrosine kinase overexpression in tumors by nuclear medicine modalities.
2008
Worms and the treatment of inflammatory bowel disease: are molecules the answer?
2008
The partitioning of PAHs to egg phospholipids facilitated by copper and proton binding via cation-pi interactions.
2007-12-15
Comparison of benzene, nitrobenzene, and dinitrobenzene 2-arylsulfenylpyrroles.
2007-09-14
Transport mechanisms for the uptake of organic compounds by rice (Oryza sativa) roots.
2007-07
Time dependence in mixture toxicity with soft electrophiles: 1. Combined effects of selected SN2- and SNAr-reactive agents with a nonpolar narcotic.
2007-04
Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation.
2007
The Elbs and Boyland-Sims peroxydisulfate oxidations.
2006-11-07
Transition state model and mechanism of nucleophilic aromatic substitution reactions catalyzed by human glutathione S-transferase M1a-1a.
2006-03-28
Interactions of nitroaromatic compounds with the mammalian selenoprotein thioredoxin reductase and the relation to induction of apoptosis in human cancer cells.
2006-03-03
PABA/NO as an anticancer lead: analogue synthesis, structure revision, solution chemistry, reactivity toward glutathione, and in vitro activity.
2006-02-09
Intermolecular electron-transfer mechanisms via quantitative structures and ion-pair equilibria for self-exchange of anionic (dinitrobenzenide) donors.
2005-05-25
"Separated" versus "contact" ion-pair structures in solution from their crystalline states: dynamic effects on dinitrobenzenide as a mixed-valence anion.
2005-02-16
Thermally-treated clay as a stationary phase in liquid chromatography.
2004-07-09
Meisenheimer complexes bonded at carbon and at oxygen.
2004-07
Sertoli cell junctional proteins as early targets for different classes of reproductive toxicants.
2004-05
Molecular optical gating devices based on polymer nanosheets assemblies.
2004-03-31
Immunotherapy of basal cell carcinoma: evolving approaches.
2003-10
Metal binding characteristics of a laterally nonsymmetric aza cryptand upon functionalization with a pi-acceptor group.
2003-08-11
Alkylation of nitroaromatics with trialkyborane.
2003-05-30
The response of adult rat sertoli cells, immortalized by a temperature-sensitive mutant of SV40, to 1,2-dinitrobenzene, 1,3-dinitrobenzene, 2,4-dinitrotoluene, 3,4-dinitrotoluene, and cadmium.
2003-04
Characterization and origin identification of 2,4,6-trinitrotoluene through its by-product isomers by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry.
2002-02-08
Chemical signatures of TNT-filled land mines.
2001-05-10
Performance evaluation of an in-injection port thermal desorption/gas chromatographic/negative ion chemical ionization mass spectrometric method for trace explosive vapor analysis.
2001-02-15
Rapid reductive destruction of hazardous organic compounds by nanoscale Fe0.
2001-02
The dynamics of blood-brain barrier breakdown in an experimental model of glial cell degeneration.
2001
Inhibition of rabbit liver monoamine oxidase by nitro aromatic compounds.
1982-08-15
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