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CAS 123812-79-3

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trans-3-Fluorocyclobutanecarboxylic acid

Description:
Trans-3-Fluorocyclobutanecarboxylic acid is a cyclic carboxylic acid characterized by its four-membered cyclobutane ring structure, which incorporates a fluorine atom at the 3-position relative to the carboxylic acid functional group. This compound exhibits unique stereochemistry due to the trans configuration, influencing its physical and chemical properties. The presence of the fluorine atom can enhance the acidity of the carboxylic group and may also affect the compound's reactivity and solubility in various solvents. Typically, such compounds can participate in various chemical reactions, including nucleophilic substitutions and acid-base reactions. The cyclobutane ring contributes to the strain in the molecule, which can lead to interesting reactivity patterns. Additionally, trans-3-fluorocyclobutanecarboxylic acid may have applications in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals where fluorinated compounds often exhibit improved biological activity. Its specific properties, such as melting point, boiling point, and solubility, would need to be determined experimentally or sourced from chemical databases for precise applications.
Formula:C5H7FO2
InChI:InChI=1/C5H7FO2/c6-4-1-3(2-4)5(7)8/h3-4H,1-2H2,(H,7,8)/t3-,4-
InChI key:InChIKey=LQXHCYIDZUPZNK-JPYJGEKTNA-N
SMILES:C(O)(=O)[C@H]1C[C@H](F)C1
Synonyms:
  • Cyclobutanecarboxylic Acid, 3-Fluoro-, Trans-
  • trans-3-Fluorocyclobutanecarboxylic acid
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