5-NITRO-O-TOLUIDINE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C7H8N2O2
Molecular Weight	152.1506
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC1=CC=C(C=C1N)[N+]([O-])=O

InChI

InChIKey=DSBIJCMXAIKKKI-UHFFFAOYSA-N

InChI=1S/C7H8N2O2/c1-5-2-3-6(9(10)11)4-7(5)8/h2-4H,8H2,1H3

HIDE SMILES / InChI

Molecular Formula	C7H8N2O2
Molecular Weight	152.1506
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
On the electron density topology and electrostatic properties of nitroanilines. A theoretical investigation on m-nitroaniline and 2-methyl-5-nitroaniline crystals.	2009-08-27	19653659
Hydrogen-bonded network in the trichloroacetate salts of 2-amino-5-chloropyridinium and 2-methyl-5-nitroanilinium monohydrate.	2009-07	19578268
A new class of functionalized polyoxometalates: synthesis, structure and preliminary antitumor activity studies of three arylimido substituted hexamolybdates bearing a strong electron-withdrawing nitro group, (Bu4N)2[Mo6O18([triple bond]NAr)] (Ar = 3-NO2-C6H4, 2-CH3-4-NO2-C6H3, 2-CH3-5-NO2-C6H3).	2008-09-21	18728886
Mobility and degradation of trinitrotoluene/metabolites in soil columns: effect of soil organic carbon content.	2008-06	18444069
[5-nitro-toluidine induced subacute poisoning hepatopathy in 3 patients].	2007-03	17498350
Phytotransformation of 2,4-dinitrotoluene in arabidopsis thaliana: toxicity, fate, and gene expression studies in vitro.	2006-12-02	17137297
Establishment of an extraction method for the recovery of tattoo pigments from human skin using HPLC diode array detector technology.	2006-09-15	16970319
Graphite-mediated reduction of 2,4-dinitrotoluene with elemental iron.	2002-05-15	12038827
Liver dysfunction among workers handling 5-nitro-o-toluidine.	2002-02	11788571
Surfactant-assisted UV-photolysis of nitroarenes.	2002-01	11838434
Biotransformation patterns of 2,4,6-trinitrotoluene by aerobic bacteria.	1998-01	9405746
Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain.	1996-07	16535348

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:42:06 GMT 2025` Edited by `admin` on `Mon Mar 31 18:42:06 GMT 2025`
Record UNII	433MYH2DWM
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

5-NITRO-O-TOLUIDINE

Common Name

English

AMARTHOL FAST SCARLET G BASE

Preferred Name

English

5-NITRO-ORTHO-TOLUIDINE

Common Name

English

5-NITRO-O-TOLUIDINE [HSDB]

Common Name

English

5-NITRO-2-TOLUIDINE

Systematic Name

English

2-AMINO-4-NITROTOLUENE

Systematic Name

English

O-TOLUIDINE, 5-NITRO-

Systematic Name

English

1-AMINO-2-METHYL-5-NITROBENZENE

Systematic Name

English

NSC-8947

Code

English

AZOIC DIAZO COMPONENT 12

Common Name

English

4-NITRO-2-AMINOTOLUENE

Systematic Name

English

3-NITRO-6-METHYLANILINE

Systematic Name

English

BENZENAMINE, 2-METHYL-5-NITRO-

Systematic Name

English

5-NITRO-ORTHO-TOLUIDINE [IARC]

Common Name

English

CI 37105

Common Name

English

2-METHYL-5-NITRO-BENZENEAMINE

Systematic Name

English

2-METHYL-5-NITROANILINE

Systematic Name

English

C.I. AZOIC DIAZO COMPONENT 12

Common Name

English

NAPHTOELAN FAST SCARLET G BASE

Brand Name

English

Code System Code Type Description

PUBCHEM

7444