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Structure of 1092961-11-9
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This bench-stable indazolylmethanol features a polar hydroxymethyl group appended to a nitrogen-rich heterocycle, enabling straightforward derivatization in synthetic and medicinal chemistry. The scaffold integrates readily into bioactive molecules, offering enhanced solubility and metabolic stability in drug discovery applications.
(1-Methyl-1H-indazol-5-yl)methanol serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient access to indazole-based scaffolds. Its primary alcohol functionality facilitates straightforward derivatization via oxidation, etherification, or esterification, while the methyl-substituted indazolyl core exhibits good bench stability and compatibility with standard coupling conditions. The compound functions effectively in parallel synthesis campaigns and supports the construction of bioactive molecules through established functional group transformations.
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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: