3-Chloro-2-nitrobenzoic acid
3-Chloro-2-nitrobenzoic acid structure
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Common Name | 3-Chloro-2-nitrobenzoic acid | ||
|---|---|---|---|---|
| CAS Number | 4771-47-5 | Molecular Weight | 201.564 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 365.6±27.0 °C at 760 mmHg | |
| Molecular Formula | C7H4ClNO4 | Melting Point | 237-239 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 174.9±23.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Synthesis and structure-activity relationships of thioflavone derivatives as specific inhibitors of the ERK-MAP kinase signaling pathway.
Bioorg. Med. Chem. 12(9) , 2397-407, (2004) Condensation of nitrobenzaldehydes 3 and alpha-[o-(p-methoxybenzylthio)benzoyl] sulfoxide 4 gave alpha-sulfinyl enones 5. Treatment of 5 with formic acid caused cyclization followed by debenzylation to afford 3-(methylsulfinyl)thioflavanones 6. Double-bond fo... |
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Hydrogen-bonded structures of the isomeric compounds of quinoline with 2-chloro-5-nitrobenzoic acid, 3-chloro-2-nitrobenzoic acid, 4-chloro-2-nitrobenzoic acid and 5-chloro-2-nitrobenzoic acid.
Acta Crystallogr. C 65(Pt 10) , o534-8, (2009) The structures of four isomeric compounds, all C7H4ClNO4.C9H7N, of quinoline with chloro- and nitro-substituted benzoic acid, namely, 2-chloro-5-nitrobenzoic acid-quinoline (1/1), (I), 3-chloro-2-nitrobenzoic acid-quinoline (1/1), (II), 4-chloro-2-nitrobenzoi... |
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The synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory activity of tacrine (Cognex®) derivaties. Gregor VE, et al.
Bioorg. Med. Chem. Lett. 2(8) , 861-4, (1992)
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