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Structure of 40353-62-6
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1-(2-Amino-5-methylthiazol-4-yl)ethanone features a reactive acetyl group attached to a 2-amino-5-methylthiazole scaffold, enabling direct incorporation into diverse heterocyclic architectures. The electron-rich thiazole ring enhances conjugation and facilitates downstream functionalization in synthetic pathways. This compound serves as a key intermediate for bioactive molecule development, particularly in medicinal chemistry applications requiring nitrogen-containing heterocycles.
1-(2-Amino-5-methylthiazol-4-yl)ethanone serves as a versatile building block for thiazole-based scaffolds, enabling efficient access to medicinally relevant heterocycles. Its amine and ketone functionalities support diverse transformations, including amidation, reductive amination, and condensation reactions. Bench-stable and readily purified, it functions effectively in standard synthetic workflows for medicinal chemistry and process development.
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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: