| Weight | 196.118 g/mol |
|---|---|
| Formula | C7H4N2O5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
2,4-Dinitrobenzaldehyde (528-75-6)
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- Elimination Reactions of (E)-2,4-Dinitrobenzaldehyde O-Aryloximes Promoted by RO-/ROH Buffers in EtOH (Journal of Organic Chemistry, 1998)
- Comparison of mutagenicity and theoretical reactivity of 2,4-dinitrobenzaldehyde and 2,6-dinitrobenzaldehyde in bacterial mutation assay and molecular orbital method. (Mutation Research Letters, 1990)
- Elimination reactions of (E)-2,4-dinitrobenzaldehyde O-benzoyloximes promoted by R2NH/R2NH2 + in 70 mol % MeCN(aq). Change of reaction mechanism (Journal of Organic Chemistry, 2008)
- Elimination Reactions of (E)-2,4-Dinitrobenzaldehyde O-Benzoyloximes. (Journal of Organic Chemistry, 1999)
- Metabolism of 2, 4-Dinitrotoluene, 2, 4-Dinitrobenzyl Alcohol and 2, 4-Dinitrobenzaldehyde by Rat Liver Microsomal and Cytosol Fractions (Chemical & Pharmaceutical Bulletin, 1987)
- Enterohepatic circulation of 2,4-dinitrobenzaldehyde, a mutagenic metabolite of 2,4-dinitrotoluene, in male Wistar rat (Xenobiotica, 1989)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])C=O
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InChIKeyZILXIZUBLXVYPI-UHFFFAOYSA-N
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