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Structure of 1003-61-8
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2-Aminothiazole-5-carbaldehyde features a reactive aldehyde group flanked by an electron-rich thiazole ring and a primary amine, enabling direct coupling in heterocyclic synthesis. This bifunctional scaffold integrates readily into bioactive molecules, offering high stability under standard conditions for medicinal chemistry applications.
2-Aminothiazole-5-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of thiazole-based heterocycles. Its dual functionality—amine and aldehyde—facilitates straightforward derivatization via reductive amination, condensation, or cyclization reactions. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for scalable synthesis and high-throughput screening applications.
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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-H317-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P272-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: