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Details

Stereochemistry ACHIRAL
Molecular Formula C6H4ClNO3
Molecular Weight 173.554
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-CHLORO-4-NITROPHENOL

SMILES

OC1=CC=C(C=C1Cl)[N+]([O-])=O

InChI

InChIKey=BOFRXDMCQRTGII-UHFFFAOYSA-N
InChI=1S/C6H4ClNO3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H

HIDE SMILES / InChI

Molecular Formula C6H4ClNO3
Molecular Weight 173.554
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Individual differences in AMY1 gene copy number, salivary α-amylase levels, and the perception of oral starch.
2010-10-13
Novel spectrofluorimetric method for measuring the activity of the enzyme alpha-L-fucosidase using the nano composite optical sensor samarium(III)-doxycycline complex doped in sol-gel matrix.
2010-07-15
Effect of GaAlAs laser irradiation on enzyme activity.
2010-06
Degradation of 4-nitrophenol, 2-chloro-4-nitrophenol, and 2,4-dinitrophenol by Rhodococcus imtechensis strain RKJ300.
2010-02-01
Spectrofluorimetric method for measuring the activity of the enzyme alpha-L-fucosidase using the ion associate of 2-chloro-4-nitro phenol-rhodamine-B.
2009-11-15
2-Chloro-1-(3-fluoro-benz-yloxy)-4-nitro-benzene.
2009-09-05
Thermophilic degradation of phenolic compounds in lab scale hybrid up flow anaerobic sludge blanket reactors.
2009-05-30
Analysis of urinary N-acetyl-beta-D-glucosaminidase using 2,4-dinitrophenyl-1-thio N-acetyl-beta-D-glucosaminide as the substrate.
2003
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:30:33 GMT 2025
Edited
by admin
on Mon Mar 31 19:30:33 GMT 2025
Record UNII
Y2V03M9UL8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-CHLORO-4-NITROPHENOL
Systematic Name English
NSC-1316
Preferred Name English
2-chlor-4-nitrophenol [WHO-DD]
Common Name English
Code System Code Type Description
PUBCHEM
12074
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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NSC
1316
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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EPA CompTox
DTXSID0060694
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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EVMPD
SUB12678MIG
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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SMS_ID
100000078293
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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FDA UNII
Y2V03M9UL8
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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CAS
619-08-9
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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ECHA (EC/EINECS)
210-578-8
Created by admin on Mon Mar 31 19:30:33 GMT 2025 , Edited by admin on Mon Mar 31 19:30:33 GMT 2025
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