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Structure of 915924-37-7
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This bench-stable oxadiazole derivative features a methyl-substituted heterocyclic core paired with a reactive hydroxymethyl group. The electron-deficient 1,3,4-oxadiazole ring enhances stability while the terminal alcohol enables straightforward derivatization. This compound serves as a versatile synthetic handle for incorporating bioactive motifs into pharmaceutical and agrochemical scaffolds.
(5-Methyl-1,3,4-oxadiazol-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling the efficient construction of oxadiazole-containing scaffolds. Its hydroxymethyl group facilitates downstream functionalization through etherification, esterification, or oxidation to aldehyde. The molecule exhibits good bench stability and compatibility with standard reaction conditions, making it well-suited for modular synthesis workflows targeting bioactive heterocycles.
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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 : H225
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Precautionary Statements : P210-P243-P273-P403
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Lot numbers can be found on the outside label of a product: