2,4-Dinitroaniline

Also known as 1-Amino-2,4-dinitrobenzene, 2,4-dinitrobenzeneamine, 2,4-dinitroaminobenzene, 2,4-dinitrobenzenamine, 2,4-Nitroaniline, 2,4-Dinitrophenylamine, 2,4-Dinitroanilina

2,4-Dinitroaniline is an organic compound with a formula of . It is used as an intermediate in the manufacturing and production of pesticides, herbicides, pharmaceuticals, and dyes. Compared to aniline, the basicity of 2,4-dinitroaniline is even weaker.

In the Vinony graph

Within Vinony's link graph, 2,4-Dinitroaniline is referenced by 7 other articles, and connects out to water, International Standard Book Number and alcohols.

It is catalogued under topics including Anilines, Chembox having GHS data and Chembox image size set.

Its subject is documented across 4 Wikipedia language editions.

Chemical data

Formula: C6H5N3O4
Molecular weight: 183.12 g/mol
IUPAC name: 2,4-dinitroaniline
SMILES: C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])N
InChIKey: LXQOQPGNCGEELI-UHFFFAOYSA-N
XLogP: 1
Polar surface area: 118 Å²
H-bond donors: 1
H-bond acceptors: 5
Formal charge: 0

via PubChem

Drug data · ChEMBL

Molecule type: Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of: chemical compound
Mass: 183.028

Show 4 more facts

canonical SMILES: C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])N
chemical formula: C₆H₅N₃O₄
melting point: 178.0
Commons category: 2,4-Dinitroaniline

Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

5 sections

Contents

Preparation and reactions
Uses
Safety
See also
References

== Preparation and reactions== 2,4-Dinitroaniline can be prepared by reaction of 1-chloro-2,4-dinitrobenzene with ammonia. It can be also prepared by the nitration of aniline.

Excerpted from Wikipedia’s “2,4-Dinitroaniline” article, available under the CC BY-SA 4.0 licence.