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Structure of 202932-04-5
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5-Methyl-2-thiazolemethanol features a thiazole core with methyl and hydroxymethyl substituents, delivering enhanced solubility and stability in polar solvents. This bench-stable scaffold integrates readily into synthetic routes for bioactive molecules, offering a robust platform for medicinal chemistry applications.
5-Methyl-2-thiazolemethanol serves as a versatile building block in medicinal chemistry, enabling efficient construction of thiazole-based scaffolds. Its pendant alcohol group facilitates derivatization via oxidation, esterification, or ether formation, while the electron-rich thiazole ring supports palladium-catalyzed cross-coupling reactions. The molecule exhibits excellent bench stability and simplifies purification due to its defined polarity profile, making it well-suited for iterative synthesis 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: