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Structure of 952182-02-4
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1H-Pyrazolo[3,4-b]pyridine-5-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 5-position, enabling direct conjugation or derivatization. This scaffold integrates rigid, electron-deficient aromaticity with a polar functional handle, enhancing solubility and enabling precise molecular positioning in medicinal chemistry and materials science applications.
1H-Pyrazolo[3,4-b]pyridine-5-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its rigid fused scaffold exhibits excellent stability and functional group tolerance, enabling direct derivatization via amide coupling, esterification, or metal-catalyzed cross-coupling reactions. The carboxylic acid moiety facilitates conjugation with biomolecules and supports purification by standard chromatographic techniques. This compound functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive scaffolds.
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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: