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Structure of 161798-01-2
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Ethyl 2-(3-formyl-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate features a uniquely functionalized thiazole core bearing both aldehyde and phenolic hydroxyl groups, enabling direct conjugation or derivatization in synthetic pathways. This bench-stable, moisture-tolerant scaffold integrates seamlessly into complex heterocyclic architectures, offering precise spatial control for medicinal chemistry and materials applications.
Ethyl 2-(3-formyl-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate serves as a versatile building block for heterocyclic synthesis, combining a reactive aldehyde, phenolic hydroxyl, and ester functionality in a single scaffold. Its formyl group enables facile imine formation and Ugi-type reactions, while the hydroxyl supports derivatization or protection strategies. The thiazole core provides structural rigidity and π-electron density beneficial for medicinal chemistry applications. Bench-stable and amenable to standard purification techniques, it facilitates efficient access to complex phenolic thiazole derivatives via multi-step transformations.
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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: