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Structure of 70958-20-2
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This acetic acid derivative features a phenoxy-substituted aryl core with a chlorine atom at the 5-position, enhancing electronic and steric properties. The pendant carboxylic acid group enables direct conjugation in synthetic routes. This structure supports efficient integration into bioactive scaffolds requiring halogenated aromatic platforms, particularly in agrochemical and pharmaceutical development workflows under standard conditions.
2-(5-Chloro-2-phenoxyphenyl)acetic acid serves as a versatile building block for the synthesis of bioactive arylacetic acid derivatives. Its structure enables straightforward functionalization at the carboxylic acid terminus and supports diverse coupling reactions, including amide formation and esterification. The phenoxy and chlorophenyl substituents confer enhanced lipophilicity and metabolic stability, making it valuable in medicinal chemistry campaigns targeting anti-inflammatory and CNS-active scaffolds. Bench-stable and readily purified by recrystallization, it functions reliably in standard 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: