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*For research and further manufacturing use only, not for direct human use.
Structure of 135242-93-2
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This triazolylmethanol delivers a versatile functional handle for conjugation and derivatization. The methyl-substituted triazole ring enhances stability and solubility, while the primary alcohol enables straightforward coupling reactions under standard conditions. Ideal for building bioconjugates and functionalized scaffolds in medicinal chemistry.
(1-Methyl-1H-[1,2,4]triazol-3-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to triazolyl-containing scaffolds via standard functional group transformations. Its bench-stable nature and compatibility with diverse reaction conditions facilitate straightforward incorporation into complex molecules. The molecule functions effectively as a linker or bioisostere in the synthesis of heterocyclic APIs and drug candidates.
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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: