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Structure of 1579295-12-7
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Methyl 2-(2-bromothiazol-5-yl)acetate features a brominated thiazole ring linked to a methyl ester-bearing acetic acid side chain. This electrophilic scaffold enables direct coupling in cross-coupling reactions and serves as a key intermediate in synthesizing bioactive heterocycles. The molecule exhibits excellent stability under standard conditions and facilitates efficient derivatization in medicinal chemistry workflows.
Methyl 2-(2-bromothiazol-5-yl)acetate serves as a versatile building block for thiazole-based scaffolds in medicinal chemistry and materials science. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports subsequent derivatization via hydrolysis or nucleophilic substitution. Bench-stable and readily purified by column chromatography, it functions efficiently in standard synthetic workflows requiring heterocyclic incorporation and functional group manipulation.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: