Diphenyl[2-(4-pyridyl)cyclopropyl]methanol

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Identification

Molecular formula
C21H19NO
CAS Number
117977-21-6
IUPAC Name
diphenyl-[2-(4-pyridyl)cyclopropyl]methanol
Molecular Weight
311.39g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1900g/cm3
Synonyms
CYPROLIDOL
Interesting facts

Interesting Facts about Diphenyl-[2-(4-pyridyl)cyclopropyl]methanol

Diphenyl-[2-(4-pyridyl)cyclopropyl]methanol is a fascinating compound with various applications in the field of organic chemistry and pharmaceuticals. Here are some engaging aspects of this compound:

  • Structural Diversity: This compound features a unique cyclopropyl ring, which is a three-membered carbon ring known for its strain and reactivity. This structure is often associated with interesting chemical behavior and synthetic methodologies.
  • Importance of Pyridine: The presence of a pyridyl group (4-pyridyl) in the molecule enhances its biological activity. Pyridine derivatives are known for their role as *ligands* in coordination chemistry and their various biological properties, including antimicrobial and antiviral activities.
  • Potential Applications: Diphenyl-[2-(4-pyridyl)cyclopropyl]methanol and its derivatives are of interest in medicinal chemistry as potential drug candidates. They may exhibit noteworthy pharmacological effects that warrant further investigation.
  • Reactivity: The cyclopropyl moiety is often used in organic synthesis due to its ability to undergo ring-opening reactions, leading to more complex structures. This feature makes it a valuable building block in creating new chemical entities.

Quote by a renowned chemist: "The beauty of organic synthesis lies in the ability to create complex molecules from simple building blocks." This quote resonates well with the study of diphenyl-[2-(4-pyridyl)cyclopropyl]methanol, a compound that exemplifies the art of molecular design.

In conclusion, diphenyl-[2-(4-pyridyl)cyclopropyl]methanol is not just another compound; it's a representation of the *intricacies of organic chemistry* that bridges structural chemistry with potential pharmacological significance. Its unique properties and functional groups underline the importance of exploring compound interactions for future innovations.

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