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Structure of 478828-52-3
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This bench-stable (1H-indazol-5-yl)methanol features a polar hydroxymethyl group appended to an electron-deficient indazole core, enabling straightforward functionalization. The scaffold integrates readily into bioactive molecule design and serves as a direct precursor for C–H oxidation or coupling reactions under standard conditions.
(1H-indazol-5-yl)methanol serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient functionalization at the indazole core. Its benzylic alcohol functionality facilitates oxidation to the aldehyde or carboxylic acid, and it participates reliably in coupling reactions such as Mitsunobu and Suzuki-Miyaura protocols. The molecule exhibits good bench stability, ease of purification, and compatibility with diverse functional groups, making it well-suited for scalable synthesis of 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 : 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: