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Structure of 893638-39-6
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5-(Pyridin-3-yl)-1,2-oxazole-3-carboxylic acid features a pyridyl moiety fused to an electron-deficient oxazole ring, enabling strong hydrogen bonding and dipole interactions. This scaffold delivers enhanced solubility and metabolic stability in bioactive molecule design. The carboxylic acid group facilitates conjugation and derivatization under standard coupling conditions.
5-(Pyridin-3-yl)-1,2-oxazole-3-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds through standard coupling and functionalization reactions. Its pyridyl-substituted oxazole core offers enhanced solubility and metabolic stability, while the carboxylic acid group facilitates direct derivatization or amide formation in peptide and macrocycle assembly. Bench-stable and readily purified by recrystallization, it functions reliably in medicinal chemistry campaigns 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: