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Structure of 885520-03-6
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5-Cyano-1H-indazole-3-carboxylic acid integrates a nitrile group and carboxylic acid functionality at distinct positions on the indazole scaffold, enabling diverse conjugation strategies. This electron-deficient heterocycle offers enhanced stability under standard conditions and serves as a key building block for bioactive molecule synthesis.
5-Cyano-1H-indazole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to indazole-based scaffolds through standard functional group transformations. Its dual functionality—cyano and carboxylic acid—supports diverse derivatization pathways, including amidation, esterification, and cyclization reactions. The compound exhibits good bench stability and facilitates purification via recrystallization or chromatography, making it well-suited for iterative synthesis campaigns in API development and target-oriented discovery.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: