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4-piperidylcyclohexyl 3-methylbutanoate

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Identification
Molecular formula
C16H29NO2
CAS number
1409774-35-4
IUPAC name
[4-(1-piperidyl)cyclohexyl] 3-methylbutanoate
State
State

At room temperature, 4-piperidylcyclohexyl 3-methylbutanoate is in a solid state. It remains stable under standard conditions and can be handled as a powder.

Melting point (Celsius)
87.00
Melting point (Kelvin)
360.15
Boiling point (Celsius)
293.00
Boiling point (Kelvin)
566.15
General information
Molecular weight
267.38g/mol
Molar mass
267.3840g/mol
Density
1.0145g/cm3
Appearence

4-piperidylcyclohexyl 3-methylbutanoate is typically present as a crystalline solid. It appears as a white or off-white powder depending on its purity and the specific conditions it has been stored.

Comment on solubility

Solubility of [4-(1-piperidyl)cyclohexyl] 3-methylbutanoate

The solubility of [4-(1-piperidyl)cyclohexyl] 3-methylbutanoate can be influenced by several factors including its molecular structure and the presence of functional groups. Generally, the compound's solubility is characterized as follows:

  • Polarity: With the piperidine ring contributing to polar characteristics, this compound may exhibit moderate solubility in polar solvents such as water and alcohols.
  • Hydrophobic regions: The cyclohexyl and methylbutanoate portions add hydrophobic characteristics, potentially reducing solubility in polar environments.
  • Solvent interactions: The compound is likely to be more soluble in organic solvents such as ethanol, acetone, or chloroform compared to water.

As a general observation, compounds similar in structure to [4-(1-piperidyl)cyclohexyl] 3-methylbutanoate:

  1. Often exhibit varying degrees of solubility based on their functional groups.
  2. Can demonstrate enhanced solubility in non-polar solvents due to their hydrophobic segments.

In conclusion, understanding the solubility of [4-(1-piperidyl)cyclohexyl] 3-methylbutanoate extends beyond simple measurements; it necessitates considering the delicate balance of polar and non-polar interactions within various solvents. As such, performing solubility tests in multiple environments is recommended to gather substantive data.

Interesting facts

Interesting Facts about [4-(1-piperidyl)cyclohexyl] 3-methylbutanoate

[4-(1-piperidyl)cyclohexyl] 3-methylbutanoate is a fascinating compound within the realm of organic chemistry, particularly due to its structural characteristics and potential applications. Here are some intriguing aspects:

  • Unique Structure: This compound is classified as an ester, derived from a carboxylic acid and an alcohol. Its structure features a cyclohexane ring, which contributes to its rigidity and unique properties.
  • Biological Relevance: Compounds resembling this structure have been studied for their pharmacological activities. The presence of a piperidine group is notable, as piperidine derivatives have shown promise in drug development, particularly in the treatment of neurological disorders.
  • Synthesis Pathways: The synthesis of esters such as this one can be achieved through various methods, including Fischer esterification or transesterification reactions, which can be essential experimental practices for chemistry students.
  • Applications in Medicinal Chemistry: Understanding compounds like [4-(1-piperidyl)cyclohexyl] 3-methylbutanoate helps researchers design new drugs that may target specific receptors in the human body, highlighting the critical intersection of organic chemistry and medicinal studies.
  • Research Opportunities: The study of this compound can lead to insights into molecular interactions, offering students and researchers avenues for experimental inquiry involving synthesis, characterization, and biological testing.

In conclusion, the exploration of [4-(1-piperidyl)cyclohexyl] 3-methylbutanoate is vital for understanding complex organic compounds and their profound implications in medicinal chemistry. Its synthetic routes, structural motifs, and potential applications make it a topic of great interest for both seasoned chemists and enthusiastic students alike.

Synonyms
ISOVALERIC ACID, 4-PIPERIDINOCYCLOHEXYL ESTER
1532-04-3
BRN 1575264
Cyclohexanol, 4-piperidino-, isovalerate
4-Piperidinocyclohexyl ester of isovaleric acid
DTXSID10165275
DTXCID7087766
(4-piperidin-1-ylcyclohexyl) 3-methylbutanoate