| Weight | 165.148 g/mol |
|---|---|
| Formula | C8H7NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4'-Nitroacetophenone (100-19-6)
4-nitroacetophenone · p-nitroacetophenone
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- Radiosensitization of mammalian cells by p-nitroacetophenone. 3. Effectiveness of nitrobenzene analogues (International Journal of Radiation Biology, 1973)
- RADIOSENSITIZATION OF MAMMALIAN CELLS BY p-NITROACETOPHENONE. I. CHARACTERIZATION IN ASYNCHRONOUS AND SYNCHRONOUS POPULATIONS. (International Journal of Radiation Biology, 1971)
- Chloramphenicol1 (Chloromycetin). VII. Synthesis through p-Nitroacetophenone (Journal of the American Chemical Society, 1949)
- The Reaction of Solvated Electrons with Cytosine, 5-methyl Cytosine and 2-deoxycytidine in Aqueous Solution the Reaction of the Electron Adduct Intermediates with Water, P-nitroacetophenone and Oxygen a Pulse Spectroscopic and Pulse Conductometric Study (International Journal of Radiation Biology, 1979)
- The Reactions of the 2-deoxyadenosine Electron Adduct in Aqueous Solution. The Effects of the Radiosensitizer p-nitroacetophenone. A Pulse Spectroscopic and Pulse Conductometric Study (International Journal of Radiation Biology, 1981)
- 4-nitroacetophenone-derived thiosemicarbazones and their copper(II) complexes with significant in vitro anti-trypanosomal activity. (European Journal of Medicinal Chemistry, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-nitroacetophenone
- p-nitroacetophenone
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SMILESCC(=O)C1=CC=C(C=C1)[N+](=O)[O-]
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InChIKeyYQYGPGKTNQNXMH-UHFFFAOYSA-N
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methyl 2-(4-nitrophenyl)acetate
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3 alternate names
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1-(2-bromo-4-nitrophenyl)ethanone
(90004-93-6)
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(67818-41-1)
3 alternate names
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3',5'-Dinitroacetophenone
(14401-75-3)
3 alternate names
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3 alternate names
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4-(4-Nitrophenyl)butyric acid
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(100-14-1)
3 alternate names
2 safety hazards
3 suppliers
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4'-Nitroacetophenone
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