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Structure of 5807-30-7
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2-(3,4-Dichlorophenyl)acetic acid features a dichlorinated aromatic ring linked to a carboxylic acid-bearing acetic acid side chain. This configuration imparts enhanced lipophilicity and metabolic stability, enabling its use in bioactive molecule synthesis. The compound serves as a key scaffold for pharmaceutical intermediates requiring halogenated phenyl functionality.
2-(3,4-Dichlorophenyl)acetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive compounds through standard carboxylic acid transformations. Its dichlorinated aromatic ring enhances metabolic stability and modulates lipophilicity, while the pendant acetic acid group facilitates derivatization via esterification, amidation, or coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in peptide conjugation, heterocycle formation, and API intermediate development.
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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: