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Structure of 27746-02-7
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4-Bromo-1H-pyrrole-2-carboxylic acid integrates a bromine substituent at the C4 position of the pyrrole ring, delivering enhanced electrophilic reactivity and stability under standard conditions. The carboxylic acid group enables direct coupling reactions or derivatization, facilitating access to diverse heterocyclic scaffolds in medicinal chemistry and materials science applications.
4-Bromo-1H-pyrrole-2-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into biologically active heterocycles. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid group supports amide formation and derivatization. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it well-suited for iterative synthesis of complex 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: