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Structure of 14903-90-3
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3-Bromofuran-2-carboxylic acid features a bromine substituent at the 3-position of a furan ring, delivering enhanced reactivity for cross-coupling and functionalization. The carboxylic acid group enables direct derivatization or incorporation into bioactive scaffolds. This bench-stable, moisture-tolerant heterocycle integrates readily into synthetic sequences requiring electron-deficient furan platforms.
3-Bromofuran-2-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent. The carboxylic acid group facilitates direct derivatization or salt formation, enhancing solubility and purification. Its bench-stable nature and compatibility with standard coupling conditions make it suitable for iterative synthesis of pharmaceutical intermediates and functionalized furan scaffolds.
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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: