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Structure of 112960-56-2
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This oxadiazole derivative features a methyl-substituted 1,2,4-oxadiazole ring linked to a primary alcohol group, offering enhanced solubility and stability under standard conditions. The methanol functionality enables straightforward derivatization in synthetic sequences. This scaffold serves as a robust bioisostere for carboxylic acids and esters in medicinal chemistry applications.
(3-Methyl-1,2,4-oxadiazol-5-yl)methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to oxadiazole-containing scaffolds prevalent in medicinal chemistry. The hydroxymethyl group facilitates downstream functionalization via esterification, etherification, or oxidation to carboxylic acid derivatives. Its bench-stable nature and compatibility with standard coupling conditions make it well-suited for modular library construction and API intermediate 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: