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Structure of 51719-65-4
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This acetic acid derivative features a 3,5-dichlorophenyl substituent that imparts enhanced lipophilicity and metabolic stability. The carboxylic acid group enables direct coupling in peptide synthesis or conjugation workflows. Bench-stable and moisture-tolerant, it serves as a robust building block for bioactive molecule design.
2-(3,5-Dichlorophenyl)acetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive compounds through standard carboxylic acid transformations. Its electron-withdrawing dichlorophenyl moiety enhances metabolic stability and modulates lipophilicity, while the benzylic position offers facile functionalization. The compound exhibits good bench stability, ease of purification, and compatibility with common coupling protocols, making it well-suited for iterative synthetic campaigns targeting pharmaceutical intermediates and heterocyclic scaffolds.
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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: