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Structure of 340736-76-7
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This trifluoromethyl-substituted oxadiazole-carboxylic acid integrates a polar, electron-deficient heterocycle with a benzoic acid handle, enabling direct conjugation in bioconjugation and medicinal chemistry. The robust oxadiazole ring enhances metabolic stability while the para-carboxylate supports derivatization under standard coupling conditions.
4-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid serves as a versatile building block for bioactive heterocycles, enabling efficient access to pharmacologically relevant scaffolds. The trifluoromethyl oxadiazole moiety imparts enhanced metabolic stability and lipophilicity, while the carboxylic acid group facilitates direct coupling reactions or derivatization. Its bench-stable nature and compatibility with standard peptide and cross-coupling protocols make it ideal for medicinal chemistry campaigns targeting CNS and oncology applications.
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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: