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Structure of 2103-94-8
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2-Amino-4-(4-bromophenyl)thiazole features a brominated phenyl group attached to a thiazole core, delivering enhanced electron-withdrawing character and improved solubility in polar organic solvents. This scaffold integrates readily into heterocyclic libraries for medicinal chemistry applications, offering a robust platform for developing kinase inhibitors and bioactive compounds under standard bench conditions.
2-Amino-4-(4-bromophenyl)thiazole serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-based heterocycles via Suzuki-Miyaura and Buchwald-Hartwig coupling reactions. The bromophenyl moiety facilitates palladium-catalyzed cross-couplings, while the amino group supports derivatization for targeted scaffold optimization. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step synthesis 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: