Weight | 198.134 g/mol |
---|---|
Formula | C7H6N2O5 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
2,4-DINITROANISOLE (119-27-7)
Score:
#205 in Environmental science
,
#4728 in Biology
,
#6017 in Chemistry
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- Sigma-Aldrich - Search for 2,4-DINITROANISOLE
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- TCI - Search for 2,4-DINITROANISOLE
- Thermophysical Properties of an Insensitive Munitions Compound, 2,4-Dinitroanisole (Journal of Chemical & Engineering Data, 2008)
- Aerobic biotransformation of 2,4-dinitroanisole in soil and soil Bacillus sp. (Biodegradation, 2012)
- Reactions of nitroanisoles. 4. Reaction of 2,4- and 2,6-dinitroanisole with cyclohexylamine. Evidence of a "dimer" nucleophile (Journal of Organic Chemistry, 1983)
- Ecotoxicological assessment of a high energetic and insensitive munitions compound: 2,4-dinitroanisole (DNAN). (Journal of Hazardous Materials, 2013)
- Environmental fate of 2,4-dinitroanisole (DNAN) and its reduced products. (Chemosphere, 2015)
- Pathways of reductive 2,4dinitroanisole (DNAN) biotransformation in sludge (Biotechnology and Bioengineering, 2013)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
-
InChIKeyCVYZVNVPQRKDLW-UHFFFAOYSA-N
- Pubchem - 2,4-DINITROANISOLE
- Wikipedia - 2,4-dinitroanisole
2,4-Dinitroanisole (DNAN) is a low sensitivity explosive organic compound. It has an anisole (methoxybenzene) core, with two nitro groups (NO2) attached. Compared with TNT it has only 90% of the explosive power and is less dense with a higher melting point.
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