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Structure of 3199-50-6
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1-(5-Bromofuran-2-yl)ethan-1-one features a brominated furan ring fused to an acetyl group, delivering high reactivity in cross-coupling and cyclization reactions. This bench-stable compound integrates readily into heterocyclic scaffolds, enabling efficient access to bioactive molecules in medicinal chemistry and materials science.
1-(5-Bromofuran-2-yl)ethan-1-one serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the furan ring via palladium-catalyzed cross-coupling reactions. The bromo substituent facilitates efficient C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the acetyl group provides a handle for further derivatization. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for constructing complex molecular architectures in medicinal chemistry and materials science workflows.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: