Structure via PubChem · Public domain (PubChem)
2,4-dinitroanisole
Sign in to saveAlso known as 2,4-Dinitro-1-methoxy-benzene, alpha-dinitroanisole, 2,4-Nitroanisole, 2,4-Dinitrophenyl methyl ether, Dinitroanisole, 2,4-Dinitrophenylmethyl ether, DNAN
2,4-Dinitroanisole (DNAN) is a low sensitivity organic compound. It has an anisole (methoxybenzene) core, with two nitro groups (–NO2) attached.
In the Vinony graph
Within Vinony's link graph, 2,4-dinitroanisole is referenced by 5 other articles, and connects out to mass density, digital object identifier and International Standard Serial Number.
It sits within the topics Chembox having GHS data, ECHA InfoCard ID from Wikidata and Explosive chemicals.
Its subject is documented across 7 Wikipedia language editions.
Chemical data
- Formula
- C7H6N2O5
- Molecular weight
- 198.13 g/mol
- IUPAC name
- 1-methoxy-2,4-dinitrobenzene
- SMILES
- COC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
- InChIKey
- CVYZVNVPQRKDLW-UHFFFAOYSA-N
- XLogP
- 2
- Polar surface area
- 101 Ų
- H-bond donors
- 0
- 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
- 198.028
Show 3 more facts
- melting point
- 91.0
- chemical formula
- C₇H₆N₂O₅
- canonical SMILES
- COC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
Sources (2)
via Wikidata · CC0
~3 min read
Encyclopedic overview
7 sectionsContents
- Properties
- Reactions
- Formation
- Use
- Environment
- See also
- References
2,4-Dinitroanisole (DNAN) is a low sensitivity organic compound. It has an anisole (methoxybenzene) core, with two nitro groups (–NO2) attached.
It is not explosive itself unless it is mixed with other explosive chemicals in certain ratios. Compared with TNT it has only 90% of the explosive power and is less dense with a higher melting point.
Excerpted from Wikipedia’s “2,4-dinitroanisole” article, available under the CC BY-SA 4.0 licence.