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Structure of 35272-15-2
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2-Methylthiazole-4-carboxylic acid features a fused thiazole ring with a methyl group at the 2-position and a carboxylic acid function at the 4-position, delivering enhanced solubility and reactivity in synthetic transformations. This scaffold integrates readily into bioactive molecules and serves as a key building block for medicinal chemistry applications.
2-Methylthiazole-4-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to thiazole-based scaffolds prevalent in medicinal chemistry. Its carboxylic acid functionality facilitates direct coupling reactions and derivatization under standard amide formation conditions. The molecule exhibits good bench stability and functional group tolerance, supporting its use in multi-step syntheses and API development workflows.
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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: