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Structure of 1805537-77-2
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This brominated difluorophenylacetic acid features a sterically accessible carboxylic acid handle flanked by electron-deficient aryl substituents, enabling direct coupling in late-stage functionalization. The ortho-bromo and para-difluoro groups facilitate transition-metal-catalyzed cross-coupling reactions under standard conditions.
2-(2-Bromo-3,6-difluorophenyl)acetic acid serves as a versatile building block for pharmaceutical intermediates, enabling efficient late-stage functionalization via its bromo and carboxylic acid functionalities. The difluorinated aryl moiety enhances metabolic stability and modulates electronic properties, while the acetic acid side chain facilitates derivatization through amide formation or esterification. Bench-stable and compatible with standard coupling protocols, it functions reliably in Suzuki-Miyaura and Stille reactions, supporting scalable synthesis of bioactive heterocycles and API candidates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: