1-carboxy-2-haloaromatic compounds
1-Carboxy-2-halogen aromatic compounds are a class of organic compounds that contain an aromatic ring with two substituents: one is a carboxyl group (-COOH) attached to the 1-position, and the other is a halogen atom (F, Cl, Br, or I) attached to the 2-position. These compounds exhibit diverse chemical reactivities due to their functional groups, making them important intermediates in various organic synthesis reactions. The carboxyl group typically participates in nucleophilic acyl substitution reactions, while the halogen can influence solubility and reactibility. Such derivatives are widely used in pharmaceuticals, agrochemicals, and materials science for their unique structural features and potential applications.
The 1-carboxy-2-haloaromatic compounds also possess good stability under mild conditions but show reactivity towards strong bases or halide-replacing agents. Their preparation often involves coupling reactions of aryl halides with carboxylic acids followed by appropriate substitution reactions to introduce the desired substituents at specific positions on the aromatic ring.
These compounds are critical in the development of new materials and drugs, where their structure can significantly impact bioavailability, efficacy, and stability.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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4-chloro-1H-pyrrole-3-carboxylic acid | 1368361-12-9 | C5H4ClNO2 |
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1,2,3,5-Tetrahydro-4,1-benzoxazepine-6-carboxylic acid;hydrochloride | 2377032-85-2 | C10H12ClNO3 |
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5-Chloro-3-phenyl-2,1-benzisoxazole-6-carboxylic acid | 41051-97-2 | C14H8ClNO3 |
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4-Bromo-2,5-dimethylpyrrole-3-carboxylic acid | 175276-47-8 | C7H8BrNO2 |
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6,8-Dimethyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylic acid;hydrochloride | 2377033-53-7 | C10H15ClN2O2 |
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4,6-Dichloropyrrolo[1,2-B]pyridazine-3-carboxylic acid | 1416440-30-6 | C8H4Cl2N2O2 |
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