5-Chloro-2-(2-(piperidin-1-yl)ethylthio)-1,3-benzoxazole

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Identification

Molecular formula
C14H15ClN2OS
CAS Number
146676-03-9
IUPAC Name
5-chloro-2-[2-(1-piperidyl)ethylsulfanyl]-1,3-benzoxazole
Molecular Weight
284.80g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3000g/cm3
Interesting facts

Interesting Facts about 5-Chloro-2-[2-(1-piperidyl)ethylsulfanyl]-1,3-benzoxazole

5-Chloro-2-[2-(1-piperidyl)ethylsulfanyl]-1,3-benzoxazole is a fascinating compound due to its structural complexity and biological significance. Here are some key points that make it remarkable:

  • Pharmacological Importance: This compound belongs to a class of substances known as benzoxazoles, which are recognized for their diverse biological activities. Research indicates that they may exhibit potential as antimicrobial, anti-inflammatory, and anticancer agents.
  • Unique Structure: The presence of a chloro group and a piperidine ring contributes to its unique chemical reactivity and interactions, making it a subject of interest in medicinal chemistry.
  • Synthesis routes: The synthesis of compounds with similar structures often involves complex organic reactions such as nucleophilic substitutions and functional group manipulations, making the study of its synthesis a valuable exercise in advanced organic chemistry.
  • Research Applications: Scholars are increasingly investigating the effects of this compound on different biological systems, including its role in neuropharmacology. The presence of the piperidine moiety suggests potential interactions with neurotransmitter systems.

As a member of a growing family of compounds with therapeutic potential, 5-chloro-2-[2-(1-piperidyl)ethylsulfanyl]-1,3-benzoxazole exemplifies the ongoing innovation in drug discovery and development. The exploration of its properties could lead to novel treatments for various diseases.

“The beauty of chemistry lies in its constant evolution; with each synthesis, we forge new pathways to understanding and healing.”

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