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Structure of 101258-16-6
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1-(2-Aminothiazol-4-yl)ethanone features a reactive thiazole amine moiety paired with a ketone group, enabling direct incorporation into bioconjugation workflows. This bench-stable compound integrates readily into synthetic scaffolds requiring nucleophilic or electrophilic handles, offering high functional group compatibility for medicinal chemistry and probe development.
1-(2-Aminothiazol-4-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling direct incorporation of the 2-aminothiazole motif into diverse molecular architectures. Its stability under standard synthetic conditions and compatibility with common coupling reactions facilitate efficient access to thiazole-containing scaffolds. The molecule functions as a key intermediate for constructing bioactive heterocycles, particularly in kinase inhibitor and antimicrobial agent development, owing to its predictable reactivity and ease of functionalization.
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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: