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Structure of 944804-79-9
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2-Amino-5-bromothiazole-4-carbonitrile features a brominated thiazole core bearing electron-rich amino and nitrile groups, enabling direct incorporation into heterocyclic scaffolds. The para-positioned nitrile facilitates conjugation and transition-metal-catalyzed coupling reactions. This bench-stable, moisture-tolerant building block supports rapid access to bioactive compounds in medicinal chemistry and materials science.
2-Amino-5-bromothiazole-4-carbonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-based heterocycles via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The molecule's orthogonal functional groups—amino, bromo, and nitrile—facilitate sequential derivatization under mild conditions, with excellent bench stability and straightforward purification. Its defined reactivity profile supports rapid scaffold diversification in API discovery workflows.
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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: