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Structure of 1353100-73-8
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Methyl 4-bromothiazole-5-carboxylate features a brominated thiazole core with a methyl ester at the C5 position, enabling direct incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates efficient cross-coupling and functionalization reactions in medicinal chemistry and materials synthesis.
Methyl 4-bromothiazole-5-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The thiazole core provides metabolic stability and structural rigidity, while the ester group offers compatibility with standard functional group manipulations. This compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: