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Structure of 29640-98-0
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This fluorinated nitroaryl acetic acid features a reactive carboxylic acid group flanked by electron-withdrawing substituents, enabling efficient coupling in peptide and pharmaceutical synthesis. The ortho-fluoro and para-nitro groups enhance electrophilicity and metabolic stability, while the bench-stable structure simplifies handling in multistep transformations.
2-(5-Fluoro-2-nitrophenyl)acetic acid serves as a versatile building block for heterocyclic synthesis and medicinal chemistry campaigns. Its ortho-nitro group enables efficient cyclization reactions, while the fluoro substituent enhances metabolic stability and modulates electronic properties. The carboxylic acid functionality facilitates direct derivatization or salt formation, offering improved solubility and purification advantages in 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-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: