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Details

Stereochemistry ACHIRAL
Molecular Formula C6H4ClNO2
Molecular Weight 157.554
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CHLORONITROBENZENE

SMILES

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

InChI

InChIKey=CZGCEKJOLUNIFY-UHFFFAOYSA-N
InChI=1S/C6H4ClNO2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H

HIDE SMILES / InChI
Molecular Formula C6H4ClNO2
Molecular Weight 157.554
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Identification of DNA adducts using HPLC/MS/MS following in vitro and in vivo experiments with arylamines and nitroarenes.
2003 Oct
[Three cases of acute p-nitrochlorobenzene poisoning].
2004 Jun
Heterogeneity of CD80 gene transcription by human keratinocytes to allergens and irritants: relevance to allergic contact dermatitis in vivo.
2004 Nov-Dec
Carcinogenicity and chronic toxicity of para-chloronitrobenzene in rats and mice by two-year feeding.
2006
Structure relationship of nitrochlorobenzene catalytic degradation process in water over palladium-iron bimetallic catalyst.
2006 Jul
Abiotic reduction of nitroaromatic compounds by aqueous iron(ll)-catechol complexes.
2006 May 1
Characterization of genes involved in the initial reactions of 4-chloronitrobenzene degradation in Pseudomonas putida ZWL73.
2006 Nov
Ethoxylation of p-chloronitrobenzene using phase-transfer catalysts by ultrasound irradiation: a kinetic study.
2007 Mar
[Effect and mechanism of removal of trace p-chloronitrobenzene in aqueous solution by ZnOOH/O3].
2007 Nov
Kinetics and mechanism of degradation of p-chloronitrobenzene in water by ozonation.
2008 Apr 15
Substituent effect on electronic structures of halonitrobenzenes.
2008 Dec 15
Abiotic reduction of nitroaromatic contaminants by iron(II) complexes with organothiol ligands.
2008 Jun
Orientational disorder in 4-chloronitrobenzene.
2008 May
Layered material gamma-ZrP supported platinum catalyst for liquid-phase reaction: a highly active and selective catalyst for hydrogenation of the nitro group in para-chloronitrobenzene.
2008 May 7
Variability of nitrogen isotope fractionation during the reduction of nitroaromatic compounds with dissolved reductants.
2008 Nov 15
Chirality change of chloronitrobenzene on Au(111) induced by inelastic electron tunneling.
2009
Degradation and detoxification of disperse dye Scarlet RR by Galactomyces geotrichum MTCC 1360.
2009 Apr
Ozone enhanced activity of aqueous titanium dioxide suspensions for photodegradation of 4-chloronitrobenzene.
2009 Aug 15
Isomerization reactions on single adsorbed molecules.
2009 Feb 17
[Simultaneous remediation of Cr (VI) and p-NCB by nanosacle iron].
2009 Jan
Bending a bond within an individual adsorbed molecule.
2009 Jan 21
1-(2-Chloro-5-nitro-phen-yl)-3-(2,2-di-methyl-propion-yl)thio-urea.
2009 Jul 1
Aqueous p-chloronitrobenzene decomposition induced by contact glow discharge electrolysis.
2009 Jul 30
Development and assessment of a rate equation for chemical transformations in reactive porous media.
2009 Jun 1
Bioaugmentation of a 4-chloronitrobenzene contaminated soil with Pseudomonas putida ZWL73.
2009 Mar
The feasibility of enhanced soil washing of p-nitrochlorobenzene (pNCB) with SDBS/Tween80 mixed surfactants.
2009 Oct 30
Patents

Patents

04041046
4
04710323
1
04801717
1
04866091
2
04987266
1
05736487
1
06307087
4
07078401
1
08722930
1
08779201
1
JP1051434A
1
JP2003321440A
1
JP2006206485A
1
JPH03101644A
1
JPH03167162A
1
JPH03232841A
1
JPH0324090A
1
JPH041232A
1
JPH04178358A
1
JPH0459751A
1
JPH05163210A
1
JPH06184060A
1
JPH07145110A
2
JPH07196643A
1
JPH07242605A
1
JPH10316635A
1
JPS51141820A
1
JPS54112830A
1
JPS5455537A
1
JPS56158740A
1
JPS5724331A
1
JPS5799301A
1
JPS5896044A
1
JPS61200947A
1
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:30:27 GMT 2023
Edited
by admin
on Fri Dec 15 18:30:27 GMT 2023
Record UNII
CVL66U249D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-CHLORONITROBENZENE
MI  
Common Name English
1-CHLORO-4-NITROBENZENE [HSDB]
Common Name English
CHLORO-4-NITROBENZENE, 1-
Systematic Name English
NSC-9792
Code English
P-CHLORONITROBENZENE [MI]
Common Name English
1-CHLORO-4-NITROBENZENE
HSDB  
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID5020281
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
CAS
100-00-5
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
HSDB
1666
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
PUBCHEM
7474
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
FDA UNII
CVL66U249D
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-809-6
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
MESH
C010407
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
MERCK INDEX
m3423
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
1-Chloro-4-nitrobenzene
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
NSC
9792
Created by admin on Fri Dec 15 18:30:27 GMT 2023 , Edited by admin on Fri Dec 15 18:30:27 GMT 2023
PRIMARY
NIH
NCATS
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