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Structure via PubChem · Public domain (PubChem)
dicloran
Sign in to saveAlso known as CNA, 1-amino-2,6-dichloro-4-nitrobenzene, 2,6-dichloro-4-nitrobenzenamine, 4-nitro-2,6-dichloroaniline, 2,6-Dichloro-4-nitroaniline
2,6-Dichloro-4-nitroaniline is an organic compound with the formula . It is the most widely discussed isomer of dichloronitroaniline, mainly as a precursor to the azo dye disperse brown 1. It is prepared by treatment of 4-nitroaniline with a mixture of hydrochloric acid and hydrogen peroxide (a source of chlorine).
In the Vinony graph
Within Vinony's link graph, dicloran is referenced by 2 other articles, and connects out to International Standard Book Number, mass density and digital object identifier.
Vinony files it under Anilines, Chembox having GHS data and Chembox image size set.
Its subject is documented across 5 Wikipedia language editions.
Chemical data
- Formula
- C6H4Cl2N2O2
- Molecular weight
- 207.01 g/mol
- IUPAC name
- 2,6-dichloro-4-nitroaniline
- SMILES
- C1=C(C=C(C(=C1Cl)N)Cl)[N+](=O)[O-]
- InChIKey
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N
- XLogP
- 2.9
- Polar surface area
- 71.8 Ų
- H-bond donors
- 1
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 205.965
- Has use
- fungicide
Show 4 more facts
- chemical formula
- C₆H₄Cl₂N₂O₂
- canonical SMILES
- C1=C(C=C(C(=C1Cl)N)Cl)[N+](=O)[O-]
- melting point
- 189.0
- Commons category
- 2,6-Dichloro-4-nitroaniline
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
2,6-Dichloro-4-nitroaniline is an organic compound with the formula . It is the most widely discussed isomer of dichloronitroaniline, mainly as a precursor to the azo dye disperse brown 1. It is prepared by treatment of 4-nitroaniline with a mixture of hydrochloric acid and hydrogen peroxide (a source of chlorine).
==References==
Excerpted from Wikipedia’s “dicloran” article, available under the CC BY-SA 4.0 licence.