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Structure of 334017-34-4
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5-(2-Chlorophenyl)isoxazole-3-carboxylic acid features a chlorinated aryl group linked to an electron-deficient isoxazole core, enabling robust integration into bioactive scaffolds. The carboxylic acid moiety offers direct handle for amidation or esterification, streamlining conjugation in medicinal chemistry campaigns. This compound exhibits enhanced metabolic stability and favorable solubility under standard conditions.
5-(2-Chlorophenyl)isoxazole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles through standard functional group transformations. Its ortho-chlorophenyl moiety enhances metabolic stability and provides a handle for further derivatization via cross-coupling reactions. The carboxylic acid functionality facilitates amide formation, esterification, and salt formation, supporting purification and formulation. Bench-stable and readily available, it functions effectively in multistep syntheses targeting pharmacologically relevant scaffolds.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: