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Structure of 3034-58-0
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5-Iodo-4-methyl-1,3-thiazol-2-amine features a reactive iodine atom at the 5-position paired with a methyl group at C4, enabling efficient cross-coupling and functionalization. The thiazole core provides enhanced stability and electron-deficient character, supporting its use in medicinal chemistry and heterocyclic synthesis. This bench-stable compound integrates readily into complex molecular architectures.
5-Iodo-4-methyl-1,3-thiazol-2-amine serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. The iodine substituent facilitates efficient C–C and C–N bond formation, while the thiazole scaffold provides metabolic stability and favorable electronic properties. Bench-stable and readily purified, it functions effectively in medicinal chemistry campaigns requiring rapid diversification of thiazole-based scaffolds.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: