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Structure of 537033-54-8
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This acetic acid derivative features a 4-bromo-2,6-difluorophenyl moiety that imparts enhanced electronic and steric control. The ortho-fluorine substituents improve metabolic stability, while the bromine enables facile cross-coupling transformations. The carboxylic acid group facilitates direct conjugation or derivatization under standard conditions. This structure serves as a key intermediate in the synthesis of bioactive molecules requiring halogenated aromatic frameworks.
2-(4-Bromo-2,6-difluorophenyl)acetic acid serves as a versatile building block for pharmaceutical intermediates, enabling efficient construction of bioactive heterocycles and substituted aryl scaffolds. Its bromo and difluoro substituents provide orthogonal reactivity for palladium-catalyzed cross-coupling and enhanced metabolic stability. The carboxylic acid group facilitates direct derivatization or salt formation, offering improved solubility and purification advantages in synthetic 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: