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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO2
Molecular Weight 137.136
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of M-NITROTOLUENE

SMILES

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

InChI

InChIKey=QZYHIOPPLUPUJF-UHFFFAOYSA-N
InChI=1S/C7H7NO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3

HIDE SMILES / InChI

Molecular Formula C7H7NO2
Molecular Weight 137.136
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dynamics of highly excited nitroaromatics.
2010-12-23
Molecular-imprinted polymer extraction combined with dispersive liquid-liquid micro-extractionfor ultra-preconcentration of mononitrotoluene.
2010-12
Electron predators are hydrogen atom traps. Effects of aryl groups on N-C(α) bond dissociations of peptide radicals.
2010-11
Evaporation and discharge dynamics of highly charged multicomponent droplets generated by electrospray ionization.
2010-01-28
A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry.
2009-11-23
Probing the mechanism of electron capture and electron transfer dissociation using tags with variable electron affinity.
2009-04-22
Femtosecond laser photoionization time-of-flight mass spectrometry of nitro-aromatic explosives and explosives related compounds.
2009-03
Kinetics and thermodynamics of sorption of nitroaromatic compounds to as-grown and oxidized multiwalled carbon nanotubes.
2009-02-01
Electrochemical destruction of dinitrotoluene isomers and 2,4,6-trinitrotoluene in spent acid from toluene nitration process.
2009-01-30
N-(3-Nitro-benzyl-idene)aniline.
2008-11-20
Voltammetric Behavior of o-Nitrophenol and Damage to DNA.
2008-03
Homogeneous liquid-liquid extraction of trace amounts of mononitrotoluenes from waste water samples.
2007-06-26
Urinary metabolites of workers exposed to nitrotoluenes.
2005-08-16
Structural insight into the dioxygenation of nitroarene compounds: the crystal structure of nitrobenzene dioxygenase.
2005-05-20
A review and assessment of hydrodynamic cavitation as a technology for the future.
2005-01
Two-dimensional correlation spectroscopy techniques applied to ion trap tandem mass spectrometric analysis: nitroaromatics.
2005
Carbon isotope fractionation during cis-trans isomerization of unsaturated fatty acids in Pseudomonas putida.
2004-12
Synthesis and dynamic NMR study of ketenimines derived from tert-butyl isocyanide, alkyl 2-arylamino-2-oxo-acetates, and dialkyl acetylenedicarboxylates.
2004
Kinetics and mechanism of the aminolysis of methyl 4-nitrophenyl, methyl 2,4-dinitrophenyl, and phenyl 2,4-dinitrophenyl carbonates.
2002-12-13
5'-substituted-6-carboxylic-2,2'-bipyridine acid: a pivotal architecton for building preorganized ligands.
2002-05-31
Theoretical study of the internal rotational barriers in nitrotoluenes, nitrophenols, and nitroanilines.
2002-01
Photocatalytic degradation of nitrotoluene in aqueous TiO2 suspension.
2002-01
Quantitative detection of aromatic compounds in single aerosol particle mass spectrometry.
2001-05-15
Comparative toxicities of o-, m-, and p-nitrotoluene in 13-week feed studies in F344 rats and B6C3F1 mice.
1994-04
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:40:26 GMT 2025
Edited
by admin
on Mon Mar 31 19:40:26 GMT 2025
Record UNII
29A9W826KQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
M-NITROTOLUENE
MI  
Systematic Name English
3-NITROTOLUENE
HSDB  
Preferred Name English
NSC-9578
Code English
1-METHYL-3-NITROBENZENE
Systematic Name English
TOLUENE, M-NITRO-
Systematic Name English
M-METHYLNITROBENZENE
Systematic Name English
M-NITROTOLUENE [MI]
Common Name English
M-MONONITROTOLUENE
Systematic Name English
MNT
Common Name English
3-METHYLNITROBENZENE
Systematic Name English
3-NITROTOLUENE [HSDB]
Common Name English
NITROTOLUENE, M-
Systematic Name English
3-METHYL-1-NITROBENZENE
Systematic Name English
Code System Code Type Description
PUBCHEM
7422
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID5021831
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-728-6
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
WIKIPEDIA
3-Nitrotoluene
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
CHEBI
39931
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
CAS
99-08-1
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
HSDB
2937
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
MERCK INDEX
m8007
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY Merck Index
NSC
9578
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
MESH
C029956
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY
FDA UNII
29A9W826KQ
Created by admin on Mon Mar 31 19:40:26 GMT 2025 , Edited by admin on Mon Mar 31 19:40:26 GMT 2025
PRIMARY