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Structure of 585-70-6
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5-Bromofuroic acid offers a strategically positioned bromine atom on the furan ring, enabling direct functionalization in cross-coupling and electrophilic substitution reactions. This electron-deficient heterocycle integrates readily into complex scaffolds, providing access to bioactive molecules and advanced materials under standard conditions.
5-Bromofuroic acid serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the 5-position of the furan ring. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid group supports derivatization via esterification, amide formation, or decarboxylative transformations. The compound exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for constructing complex heterocyclic scaffolds and pharmaceutical intermediates.
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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 : H319
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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: