Lidocaine

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Identification

Molecular formula
C17H27NO2
CAS Number
137-58-6
IUPAC Name
2-(diethylamino)ethyl 2,2-diphenylpentanoate
Molecular Weight
324.45g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0260g/cm3
Synonyms
proadifen
Interesting facts

Exploring 2-(diethylamino)ethyl 2,2-diphenylpentanoate

2-(diethylamino)ethyl 2,2-diphenylpentanoate, often referred to in scientific literature as a compound with significant relevance in medicinal chemistry, showcases intriguing properties and applications that capture the interest of chemists. Here are some engaging aspects of this compound:

  • Structural Diversity: The molecular architecture of 2-(diethylamino)ethyl 2,2-diphenylpentanoate features a unique combination of functionalities, including a diethylamino group and a branched pentanoate chain, which contribute to its potential bioactivity.
  • Pharmacological Potential: Compounds like 2-(diethylamino)ethyl 2,2-diphenylpentanoate are often investigated for their role in drug design, particularly for their effects on the central nervous system. The presence of the amino group enhances its capability to cross the blood-brain barrier, positioning it as a candidate for developing therapeutics.
  • Synthetic Methodology: The synthesis of this compound can be achieved through several organic reactions, demonstrating students' skills in multi-step synthesis. Understanding these processes boosts practical laboratory experience and theoretical knowledge.
  • Research Implications: Scientists are continuously studying this class of compounds for antidepressant and anesthetic properties, which are crucial in medicine. The exploration of analogs can yield substances with even refined characteristics and potency.

As we delve into the world of organic chemistry, compounds such as 2-(diethylamino)ethyl 2,2-diphenylpentanoate remind us of the profound connection between molecular structure and biological activity, highlighting the endless possibilities that await discovery in chemical research.

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