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Structure of 2089381-00-8
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6-Bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carboxylic acid features a fused heterocyclic core bearing bromo and methoxy substituents at electron-rich positions, enabling direct functionalization in cross-coupling reactions. The carboxylic acid group provides a handle for amide bond formation or salt generation, enhancing solubility and bioavailability. This scaffold exhibits stability under standard reaction conditions, facilitating use in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
6-Bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carboxylic acid serves as a versatile building block for the synthesis of biologically active heterocycles. Its bromo and carboxylic acid functionalities enable palladium-catalyzed cross-coupling and derivatization reactions, while the methoxy group provides orthogonal reactivity. The molecule exhibits good bench stability and facilitates efficient purification, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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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: