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Structure of 860496-20-4
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1H-Pyrrolo[3,2-b]pyridine-3-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 3-position, enabling direct conjugation or derivatization in synthetic routes. The electron-deficient pyrrolopyridine scaffold enhances reactivity in cross-coupling and cyclization processes, while the acidic proton supports salt formation for improved solubility and handling. This structure serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
1H-Pyrrolo[3,2-b]pyridine-3-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its rigid fused scaffold enables predictable bioactive conformation and facilitates functionalization at the carboxylic acid terminus. The molecule exhibits good bench stability, moderate solubility in common organic solvents, and compatibility with standard coupling reactions, including amide formation and esterification, supporting efficient access to diverse analogs in lead optimization campaigns.
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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: