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Structure of 331-41-9
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2-(4-Chloro-3-fluorophenoxy)acetic acid features a strategically positioned chloro-fluoro substituent on the phenyl ring, enhancing electron-withdrawal and metabolic stability. This derivative integrates readily into bioactive scaffolds, particularly in agrochemical development where its lipophilic character supports membrane permeability and target engagement.
2-(4-Chloro-3-fluorophenoxy)acetic acid serves as a versatile building block for the synthesis of bioactive molecules, particularly in agrochemical and pharmaceutical research. Its ortho-halogenated phenoxy scaffold enables efficient coupling reactions, while the carboxylic acid group facilitates derivatization via esterification, amidation, or salt formation. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for use in multi-step syntheses requiring functional group tolerance and predictable reactivity.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: