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Structure of 33282-16-5
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This isoxazole derivative features a para-methoxyphenyl group that enhances solubility and modulates electronic properties. The carboxylic acid functionality enables direct conjugation or derivatization in synthetic routes. Designed for stability under standard conditions, it integrates efficiently into bioactive scaffolds and serves as a key intermediate in medicinal chemistry campaigns targeting heterocyclic frameworks.
5-(4-Methoxyphenyl)isoxazole-3-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds via standard coupling and functionalization reactions. The isoxazole core exhibits excellent bench stability and compatibility with diverse reaction conditions, while the carboxylic acid functionality facilitates direct amidation, esterification, or metal-catalyzed cross-coupling. Its methoxy-substituted aryl group enhances solubility and provides a handle for further derivatization, making it well-suited for medicinal chemistry and process development workflows.
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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 : H319
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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: