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Structure of 74205-82-6
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(1H-1,2,4-Triazol-1-yl)methanol features a reactive triazolylmethyl handle ideal for coupling reactions in medicinal chemistry and materials synthesis. The molecule integrates readily into functional scaffolds due to its polar yet stable nature, enabling efficient derivatization under mild conditions.
(1H-1,2,4-Triazol-1-yl)methanol serves as a versatile building block for constructing triazolyl-containing scaffolds in medicinal chemistry and materials science. Its hydroxymethyl group enables straightforward derivatization via etherification, esterification, or substitution reactions, while the triazole ring offers excellent stability and hydrogen-bonding capability. The compound exhibits good bench stability and is compatible with a range of functional groups, facilitating its use in multi-step syntheses and high-throughput library generation.
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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: