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Structure of 64132-13-4
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This bench-stable indazolylmethanol features a polar hydroxymethyl group attached to an electron-rich heterocyclic core, enabling direct functionalization in late-stage synthesis. Its compatibility with diverse reaction conditions supports efficient integration into bioactive scaffolds and medicinal chemistry libraries.
(1H-Indazol-3-yl)methanol serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling direct functionalization at the indazole core. Its benzylic alcohol functionality facilitates oxidation to carboxylic acids, substitution to form ethers or esters, and coupling reactions under standard conditions. The molecule exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for multi-step synthesis campaigns in API development.
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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: