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Structure of 4175-66-0
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2,5-Dimethylthiazole serves as a valuable heterocyclic scaffold in medicinal chemistry and synthetic methodology. This bench-stable, electron-rich thiazole derivative features methyl groups at the 2- and 5-positions, enhancing its lipophilicity and metabolic stability. It integrates readily into bioactive molecules, particularly in kinase inhibitors and antiparasitic agents. The fused ring system provides a rigid, planar framework ideal for target engagement.
2,5-Dimethylthiazole serves as a versatile heterocyclic building block in medicinal chemistry and catalyst design. Its stable, electron-rich core facilitates palladium-catalyzed cross-coupling reactions and functions as a key scaffold in bioactive molecule synthesis. The methyl groups enhance solubility and metabolic stability, while the thiazole ring provides robustness under standard reaction conditions. This compound enables efficient access to complex architectures via functionalization at C-4 or C-2 positions.
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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: