| Bioactivity | 4-Chloro-3-nitrobenzoic acid has oral activity, and oral administration can affect the synthesis activity of liver proteins and the activities of urokinase and histidine kinase[1][2]. | ||||||||||||
| CAS | 96-99-1 | ||||||||||||
| Formula | C7H4ClNO4 | ||||||||||||
| Molar Mass | 201.56 | ||||||||||||
| Appearance | 固体 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
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| Reference | [1]. Thompson AJ, et al. The mechanism of bending in co-crystals of caffeine and 4-chloro-3-nitrobenzoic acid. Nat Commun. 2021 Oct 20;12(1):5983. [2]. D'eng B, et al. Otsenka gepatotoksicheskogo deĭstviia nekotorykh khlor- nitroproizvodnykh benzoĭnoĭ kisloty [Evaluation of the hepatotoxic activity of several chlor-nitro derivatives of benzoic acid]. Vopr Med Khim. 1983 Nov-Dec;29(6):113-7. Russian. |
4-Chloro-3-nitrobenzoic acid
CAS: 96-99-1 F: C7H4ClNO4 W: 201.56
4-Chloro-3-nitrobenzoic acid has oral activity, and oral administration can affect the synthesis activity of liver prote
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