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- Molecular formula
- C13H19NO2
- CAS Number
- 536-33-4
- IUPAC Name
- 2-(2-piperidyl)ethyl 2-methylprop-2-enoate
- Molecular Weight
- 219.30g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0564g/cm3
- Synonyms
- 2-Piperidinoethyl methacrylate
Identification
Interesting facts
Interesting Facts about 2-(2-piperidyl)ethyl 2-methylprop-2-enoate
2-(2-piperidyl)ethyl 2-methylprop-2-enoate is a fascinating compound with numerous applications and attributes that make it noteworthy in the field of chemistry:
- Chemical Structure: This compound features a unique structure that includes a piperidine ring, which is known for its significant contributions to medicinal chemistry. The presence of this cyclic amine allows for interesting interactions in biological systems.
- Potential Biological Activity: Compounds featuring the piperidine moiety often exhibit a range of biological activities, including analgesic, antihistaminic, and antipsychotic effects, making them valuable in drug discovery and development.
- Versatile Reactivity: The presence of the 2-methylprop-2-enoate group opens up numerous avenues for further chemical transformations. This characteristic significantly enhances its utility in synthetic organic chemistry.
- Synthesis Methods: Various synthetic routes can lead to the formation of this compound, including the use of Michael additions or esterifications, allowing chemists to explore different pathways and improve yields.
- Research Impact: The exploration of this compound, alongside derivatives of piperidine and acrylic acid esters, continues to inspire research aimed at discovering new pharmacological properties and improving existing synthetic methods.
In summary, 2-(2-piperidyl)ethyl 2-methylprop-2-enoate exemplifies how a simple change in structure can lead to vast implications in both synthetic and medicinal chemistry. This compound not only serves as a building block in various syntheses but also beckons scientists to delve deeper into its biologically relevant properties.