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Structure of 24068-60-8
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Methyl 2-(3-bromoisoxazol-5-yl)acetate features a brominated isoxazole ring fused to an ester-functionalized acetic acid derivative, delivering high reactivity in cross-coupling and heterocyclic synthesis. This bench-stable reagent integrates readily into complex molecular architectures, enabling efficient access to bioactive scaffolds with enhanced metabolic stability.
Methyl 2-(3-bromoisoxazol-5-yl)acetate serves as a versatile building block for constructing brominated isoxazole-containing scaffolds. The pendant bromine enables direct functionalization via palladium-catalyzed cross-coupling reactions, while the ester group facilitates subsequent transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthesis in medicinal chemistry and API development 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: