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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

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative toxicities of o-, m-, and p-nitrotoluene in 13-week feed studies in F344 rats and B6C3F1 mice.
1994 Apr
Kinetics and mechanism of the aminolysis of methyl 4-nitrophenyl, methyl 2,4-dinitrophenyl, and phenyl 2,4-dinitrophenyl carbonates.
2002 Dec 13
Theoretical study of the internal rotational barriers in nitrotoluenes, nitrophenols, and nitroanilines.
2002 Jan
5'-substituted-6-carboxylic-2,2'-bipyridine acid: a pivotal architecton for building preorganized ligands.
2002 May 31
Synthesis and dynamic NMR study of ketenimines derived from tert-butyl isocyanide, alkyl 2-arylamino-2-oxo-acetates, and dialkyl acetylenedicarboxylates.
2004
Two-dimensional correlation spectroscopy techniques applied to ion trap tandem mass spectrometric analysis: nitroaromatics.
2005
A review and assessment of hydrodynamic cavitation as a technology for the future.
2005 Jan
Homogeneous liquid-liquid extraction of trace amounts of mononitrotoluenes from waste water samples.
2007 Jun 26
N-(3-Nitro-benzyl-idene)aniline.
2008 Nov 20
Probing the mechanism of electron capture and electron transfer dissociation using tags with variable electron affinity.
2009 Apr 22
Electrochemical destruction of dinitrotoluene isomers and 2,4,6-trinitrotoluene in spent acid from toluene nitration process.
2009 Jan 30
A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry.
2009 Nov 23
Molecular-imprinted polymer extraction combined with dispersive liquid-liquid micro-extractionfor ultra-preconcentration of mononitrotoluene.
2010 Dec
Dynamics of highly excited nitroaromatics.
2010 Dec 23
Evaporation and discharge dynamics of highly charged multicomponent droplets generated by electrospray ionization.
2010 Jan 28
Electron predators are hydrogen atom traps. Effects of aryl groups on N-C(α) bond dissociations of peptide radicals.
2010 Nov
Patents
Name Type Language
M-NITROTOLUENE
MI  
Systematic Name English
NSC-9578
Code English
3-NITROTOLUENE
HSDB  
Systematic Name 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 Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID5021831
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-728-6
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
WIKIPEDIA
3-Nitrotoluene
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
CHEBI
39931
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
CAS
99-08-1
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
HSDB
2937
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
MERCK INDEX
m8007
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY Merck Index
NSC
9578
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
MESH
C029956
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY
FDA UNII
29A9W826KQ
Created by admin on Fri Dec 15 19:15:15 GMT 2023 , Edited by admin on Fri Dec 15 19:15:15 GMT 2023
PRIMARY