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Structure of 1031417-77-2
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1-Methyl-1H-indazole-6-carboxylic acid features a polar carboxylic acid group attached to a nitrogen-rich indazole scaffold, enabling direct conjugation or derivatization in medicinal chemistry. This derivative combines enhanced solubility with metabolic stability, making it ideal for probing bioactive heterocycles in drug discovery workflows.
1-Methyl-1H-indazole-6-carboxylic acid serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient incorporation into bioactive scaffolds. Its well-defined reactivity supports direct derivatization via amide coupling, esterification, and decarboxylation protocols. The molecule exhibits bench stability, good solubility in common organic solvents, and functional group tolerance, facilitating straightforward purification and integration into multi-step syntheses.
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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: