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Structure of 75908-73-5
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2-(4-Fluorophenyl)propanoic acid features a fluorinated aromatic ring paired with a chiral aliphatic carboxylic acid moiety, enabling its use in asymmetric synthesis and medicinal chemistry. This bench-stable compound integrates readily into pharmaceutical intermediates requiring electron-withdrawing fluorine substitution and enhanced metabolic stability.
2-(4-Fluorophenyl)propanoic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive compounds through standard coupling and functionalization reactions. Its fluorinated aromatic moiety enhances metabolic stability and modulates lipophilicity, while the α-methyl carboxylic acid functionality offers reliable reactivity in amide bond formation, esterification, and decarboxylation processes. The compound exhibits excellent bench stability and is readily purified by recrystallization, facilitating its use in scalable synthetic routes.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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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: