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Structure of 2527-99-3
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Methyl 5-bromofuran-2-carboxylate is a bench-stable, moisture-tolerant heterocyclic ester featuring a bromine substituent at the 5-position of the furan ring. This electron-deficient scaffold integrates readily into transition-metal-catalyzed cross-coupling reactions, enabling efficient access to functionalized furan derivatives for medicinal chemistry and materials science applications.
Methyl 5-bromofuran-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent. The furan ring provides a platform for electrophilic functionalization and further derivatization, while the ester group offers compatibility with standard reduction and nucleophilic substitution protocols. Its bench-stable nature and predictable reactivity make it suitable for iterative synthetic sequences in medicinal chemistry and process 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 : 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: