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ETH-LAD

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Identification
Molecular formula
C25H35NO3
CAS number
65527-62-0
IUPAC name
ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate
State
State
At room temperature, ETH-LAD is typically found in a solid form.
Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
479.36
Boiling point (Kelvin)
752.51
General information
Molecular weight
404.58g/mol
Molar mass
404.5790g/mol
Density
1.0885g/cm3
Appearence

This compound appears as a solid at room temperature, though specific details on its color or crystal structure are not widely documented.

Comment on solubility

Solubility of Ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate

The solubility of ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate can be influenced by various factors, including its molecular structure and the presence of functional groups. This compound features both hydrophilic and hydrophobic characteristics, which play a crucial role in its overall solubility profile.

Here are some key points regarding its solubility:

  • Hydrophobic nature: The presence of the phenyl group and the tetrahydrofuran ring contributes to a non-polar character, suggesting lower solubility in water.
  • Possible polar interactions: The carboxylate functional group may enhance solubility in polar solvents, promoting interactions with water molecules.
  • Solvent choice: The solubility will likely be greater in organic solvents, such as ethanol or methanol, compared to aqueous environments.
  • Temperature dependency: Temperature variations can also affect solubility, often leading to increased solubility in higher temperatures.

Overall, while ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate demonstrates complex solubility behavior due to its distinct structural features, one can anticipate a broader solubility range in organic solvents compared to water. Thus, understanding its behavior in different solvent systems is essential for effective utilization in synthetic processes or applications.

Interesting facts

Interesting Facts About Ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate

Ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate is a fascinating compound, particularly within the realm of medicinal chemistry. It showcases unique structural features and potential therapeutic applications that highlight its importance in the development of novel pharmaceutical agents.

Key Characteristics

  • Structural Complexity: The compound possesses a piperidine ring, which is well-known for its presence in many biologically active molecules. The combination of the piperidine with aromatic and cyclic structures lends complexity to its chemical behavior.
  • Potential Pharmacological Applications: Compounds with similar structures have been investigated for their effects as analgesics, anxiolytics, and anti-depressants. The structural diversity may confer unique mechanisms of action.
  • Biological Activity Exploration: Research into compounds resembling ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate can yield insights into drug interactions with neural receptors and other biological pathways.

Scientific Implications

As a researcher or student delving into organic chemistry and pharmacology, one might find the synthesis of this compound particularly intriguing. The following points exemplify its significance:

  • Drug Development: Understanding how variations in the molecular structure alter activity can lead to tailored therapeutic approaches.
  • Interdisciplinary Research: The study of this compound could involve a collaboration between organic chemists, pharmacologists, and toxicologists.
  • Novel Synthesis Techniques: Synthesis of such compounds often requires innovative methodologies, which can push the boundaries of what is commonly practiced in labs.

Overall, ethyl 4-phenyl-1-(4-tetrahydrofuran-2-ylbutyl)piperidine-4-carboxylate stands as a prime example of how organic compounds are interwoven with the challenges and triumphs of medicinal chemistry. As researchers continue to explore its potential, we may uncover significant advancements in therapeutic strategies that can improve patient outcomes.

Synonyms
2260-46-0
4-Phenyl-1-(4-(tetrahydro-2-furyl)butyl)isonipecotic acid ethyl ester
TA 103
BRN 0442088
ethyl 1-[4-(oxolan-2-yl)butyl]-4-phenylpiperidine-4-carboxylate
4-Piperidinecarboxylic acid, 4-phenyl-1-(4-(tetrahydro-2-furanyl)butyl)-, ethyl ester
ISONIPECOTIC ACID, 4-PHENYL-1-(4-(TETRAHYDRO-2-FURYL)BUTYL)-, ETHYL ESTER
DTXSID90945259