Flurbiprofen

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Identification

Molecular formula
C15H13FO2
CAS Number
5104-49-4
IUPAC Name
2-[4-(2-fluorophenyl)phenyl]acetic acid
Molecular Weight
244.27g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2500g/cm3
Synonyms
5001-99-0
Interesting facts

Interesting Facts about 2-[4-(2-Fluorophenyl)phenyl]acetic Acid

2-[4-(2-Fluorophenyl)phenyl]acetic acid is a fascinating compound that has drawn attention in the fields of medicinal chemistry and organic synthesis. Here are some intriguing points about this compound:

  • Structural Complexity: The compound's structure features two aromatic rings, which contribute to its unique chemical behavior and interactions. The substitution of a fluorine atom plays a vital role in altering both its physical and chemical properties.
  • Pharmacological Potential: Due to its structural resemblance to non-steroidal anti-inflammatory drugs (NSAIDs), research has been conducted to explore its potential therapeutic applications, particularly in pain management and inflammation.
  • Fluorine Influence: The presence of a fluorine atom often enhances the biological activity of compounds. This characteristic is attributed to fluorine's electronegativity, potentially influencing binding affinity to biological targets.
  • Synthetic Routes: The synthesis of 2-[4-(2-fluorophenyl)phenyl]acetic acid generally involves advanced organic chemistry techniques, showcasing the creativity and skills of chemists in constructing complex molecules from simpler precursors.
  • Applications in Research: This compound is frequently used in scientific research as a model to study molecular interactions, drug efficacy, and the development of new therapeutic agents.

As an individual interested in chemistry, one might say: "The exploration of compounds like 2-[4-(2-fluorophenyl)phenyl]acetic acid not only enhances our understanding of chemical structures but also opens doors to groundbreaking advancements in pharmaceuticals." The ongoing study of this compound reflects the dynamic and ever-evolving nature of chemical science.

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