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Structure of 53159-71-0
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1-(2-Aminothiazol-5-yl)ethanone features a reactive acetyl group flanked by a nitrogen-rich thiazole ring, enabling direct incorporation into bioactive scaffolds. This bench-stable derivative serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and antimicrobial agents.
1-(2-Aminothiazol-5-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-based scaffolds. Its amine and ketone functionalities support diverse transformations, including nucleophilic additions, amidations, and condensation reactions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns 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 : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: