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Structure of 202000-99-5
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This brominated fluorophenylacetic acid features a strategically positioned bromine and fluorine substituent, enabling selective coupling reactions in medicinal chemistry. The carboxylic acid group facilitates derivatization, while the electron-withdrawing halogens enhance reactivity in cross-coupling processes. Designed for synthetic precision, this intermediate supports efficient access to complex bioactive architectures under standard conditions.
2-(3-Bromo-5-fluorophenyl)acetic acid serves as a versatile building block for the synthesis of pharmaceutical intermediates and bioactive heterocycles. Its ortho-halogenated aryl motif enables efficient Pd-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates derivatization via amide, ester, or acyl chloride formation. The molecule exhibits excellent bench stability and compatibility with standard purification techniques, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development workflows.
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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: