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Structure of 1557370-29-2
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1-Fluorocyclopentanecarboxylic acid features a fluorinated cyclopentane ring that imparts enhanced metabolic stability and lipophilicity, making it valuable for medicinal chemistry applications. The carboxylic acid group enables direct derivatization or salt formation, facilitating incorporation into bioactive molecules. This bench-stable, moisture-tolerant reagent streamlines the synthesis of fluorinated analogs in drug discovery workflows.
1-Fluorocyclopentanecarboxylic acid serves as a valuable building block in medicinal chemistry, enabling the introduction of a fluorinated cyclopentane motif into bioactive molecules. The carboxylic acid functionality facilitates direct derivatization via amide, ester, or acyl chloride formation, while the adjacent fluorine atom provides metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for use in peptide conjugation, heterocycle synthesis, and the construction of pharmacologically relevant 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: