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Structure of 194240-75-0
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4-Chloro-2-fluorophenylacetic acid features a strategically positioned chloro and fluoro substituent on the phenyl ring, enhancing electronic effects and metabolic stability. This electron-deficient aryl moiety integrates readily into bioactive scaffolds, offering improved binding affinity in medicinal chemistry applications. The carboxylic acid group enables direct conjugation or derivatization under standard conditions.
4-Chloro-2-fluorophenylacetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive compounds through standard coupling and functionalization reactions. Its electron-withdrawing halogen substituents enhance metabolic stability and modulate electronic properties. The carboxylic acid group facilitates direct derivatization or incorporation into peptide and heterocyclic scaffolds, offering excellent bench stability and compatibility with common purification methods.
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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: