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Structure of 709608-85-5
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4-(Hydroxymethyl)-1H-indazole features a reactive hydroxymethyl group positioned at the 4-position of the indazole scaffold, enabling direct functionalization in synthetic transformations. This bench-stable heterocycle integrates readily into bioconjugation strategies and serves as a key intermediate for pharmaceutical development.
4-(Hydroxymethyl)-1H-indazole serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling straightforward functionalization at the C4 position. The hydroxymethyl group facilitates oxidation to carboxylic acid, reduction to methyl, or conversion to other polar functionalities, supporting diverse downstream derivatization. Its stability under standard reaction conditions and compatibility with common protecting group strategies make it well-suited for multi-step synthesis workflows 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: