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Structure of 98027-21-5
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2-Aminothiazole-4-carbonitrile features a dual functional group architecture combining an amine and a nitrile at the 2- and 4-positions of the thiazole ring. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct incorporation into bioactive scaffolds through nucleophilic or coupling reactions. The molecule exhibits enhanced solubility in polar solvents and stability under standard bench conditions.
2-Aminothiazole-4-carbonitrile serves as a versatile building block in medicinal chemistry, enabling efficient construction of thiazole-based heterocycles. Its dual functionality—amine and nitrile groups—facilitates diverse transformations, including nucleophilic additions, cyclizations, and coupling reactions. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for use in multi-step synthesis workflows targeting API scaffolds.
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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: