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Structure of 59660-30-9
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This bench-stable triazolylmethanol features a methyl-substituted triazole ring that enhances electron density and solubility in polar solvents. The primary alcohol functionality enables direct coupling or derivatization in synthetic workflows. It serves as a versatile scaffold for bioactive molecule construction and functional material development.
(4-Methyl-4H-1,2,4-triazol-3-yl)methanol serves as a versatile building block for the synthesis of triazolyl-containing heterocycles and bioactive molecules. Its hydroxymethyl functionality enables straightforward derivatization via etherification, esterification, or oxidation to aldehyde, facilitating downstream conjugation and scaffold elaboration. The molecule exhibits good bench stability and functional group tolerance, making it suitable for use in iterative synthetic sequences and medicinal chemistry campaigns.
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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: