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Structure of 1030613-07-0
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5-Bromo-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester features a brominated thiadiazole core that enables direct functionalization in heterocyclic synthesis. This bench-stable, moisture-tolerant reagent integrates readily into cross-coupling and cyclization workflows, delivering access to bioactive nitrogen- and sulfur-containing scaffolds with high regiocontrol.
5-Bromo-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The bromo substituent enables palladium-catalyzed cross-coupling reactions, while the ester group supports selective hydrolysis or further derivatization. This compound exhibits good bench stability, facilitates purification via standard chromatographic methods, and functions effectively in constructing bioactive [1,3,4]thiadiazole scaffolds relevant to pharmaceutical development.
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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: