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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO3
Molecular Weight 153.1354
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-NITRO-M-CRESOL

SMILES

CC1=CC(O)=C(C=C1)[N+]([O-])=O

InChI

InChIKey=NQXUSSVLFOBRSE-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4,9H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Mutagenic activities of a chlorination by-product of butamifos, its structural isomer, and their related compounds.
2010-01
Investigations on the gas-phase photolysis and OH radical kinetics of methyl-2-nitrophenols.
2007-11-14
Abatement and degradation pathways of toluene in indoor air by positive corona discharge.
2007-08
Pairwise-substitution effects and intramolecular hydrogen bonds in nitrophenols and methylnitrophenols. Thermochemical measurements and ab initio calculations.
2007-07-19
Spatial and geographical variations of urban, suburban and rural atmospheric concentrations of phenols and nitrophenols.
2006-03
Simultaneous determination of montelukast and loratadine by HPLC and derivative spectrophotometric methods.
2003-02-26
Simultaneous determination of fexofenadine and its related compounds by HPLC.
2002-07-20
Patents
Name Type Language
6-NITRO-M-CRESOL
Systematic Name English
NSC-3142
Preferred Name English
3-METHYL-6-NITROPHENOL
Systematic Name English
NITRO-M-CRESOL, 6-
Systematic Name English
2-NITRO-5-METHYLPHENOL
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
211-843-0
Created by admin on Mon Mar 31 18:58:24 GMT 2025 , Edited by admin on Mon Mar 31 18:58:24 GMT 2025
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CAS
700-38-9
Created by admin on Mon Mar 31 18:58:24 GMT 2025 , Edited by admin on Mon Mar 31 18:58:24 GMT 2025
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NSC
3142
Created by admin on Mon Mar 31 18:58:24 GMT 2025 , Edited by admin on Mon Mar 31 18:58:24 GMT 2025
PRIMARY
PUBCHEM
12788
Created by admin on Mon Mar 31 18:58:24 GMT 2025 , Edited by admin on Mon Mar 31 18:58:24 GMT 2025
PRIMARY
EPA CompTox
DTXSID00220261
Created by admin on Mon Mar 31 18:58:24 GMT 2025 , Edited by admin on Mon Mar 31 18:58:24 GMT 2025
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FDA UNII
Z0B5EO9752
Created by admin on Mon Mar 31 18:58:24 GMT 2025 , Edited by admin on Mon Mar 31 18:58:24 GMT 2025
PRIMARY