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Ethyl 1-allyl-4-phenylpiperidine-4-carboxylate

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Identification
Molecular formula
C17H23NO2
CAS number
40527-18-8
IUPAC name
ethyl 1-allyl-4-phenyl-piperidine-4-carboxylate
State
State

At room temperature, ethyl 1-allyl-4-phenylpiperidine-4-carboxylate is typically found in a liquid state.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
312.00
Boiling point (Kelvin)
585.15
General information
Molecular weight
259.37g/mol
Molar mass
259.3690g/mol
Density
1.0400g/cm3
Appearence

Ethyl 1-allyl-4-phenylpiperidine-4-carboxylate typically appears as a colorless to pale yellow liquid. This organic compound, like many others within the piperidine family, may have a characteristic mild odor.

Comment on solubility

Solubility of Ethyl 1-allyl-4-phenyl-piperidine-4-carboxylate

Ethyl 1-allyl-4-phenyl-piperidine-4-carboxylate is a fascinating compound with distinct solubility characteristics that can be influenced by various factors.

Key Factors Influencing Solubility:

  • Polar vs. Non-Polar: The presence of both polar and non-polar functional groups in its structure may lead to moderate solubility in polar solvents like ethanol or methanol, while potentially showing less solubility in non-polar solvents.
  • Temperature: Solubility can often increase with temperature; thus, heating this compound in suitable solvents might improve its dissolution.
  • pH Levels: The ionization state of the compound could be affected by the pH of the solvent, which may affect its solubility in aqueous solutions.

It is often described that "like dissolves like," indicating that the solubility of ethyl 1-allyl-4-phenyl-piperidine-4-carboxylate will be higher in solvents that share similar polarity to its functional groups.

Ultimately, while precise solubility data may vary based on experimental conditions, understanding these factors can provide a valuable framework for predicting the behavior of this compound in different environments.

Interesting facts

Interesting Facts about Ethyl 1-Allyl-4-Phenyl-Piperidine-4-Carboxylate

Ethyl 1-allyl-4-phenyl-piperidine-4-carboxylate is a fascinating compound that belongs to the category of piperidine derivatives, which are widely studied for their numerous applications in medicinal chemistry. Here are some engaging insights:

  • Pharmaceutical Relevance: This compound is part of a larger family of piperidine compounds, many of which exhibit significant biological activities. Its structure may contribute to potential therapeutic effects, making it a subject of interest in drug development.
  • Structural Features: The unique combination of an allyl group and a phenyl group attached to the piperidine ring provides interesting properties that can influence the compound's reactivity and interactions.
  • Application in Synthesis: Ethyl 1-allyl-4-phenyl-piperidine-4-carboxylate can serve as a versatile intermediate in organic synthesis, paving the way for the creation of various complex molecules.
  • Mechanistic Insights: Understanding the electronic properties of the piperidine ring and the substituents can offer valuable insights into its mechanisms of action and potential pathways for chemical reactions.
  • Research Potential: Ongoing research in this area could lead to the discovery of new compounds that have enhanced efficacy or reduced side effects, making it a promising avenue for future exploration.

In conclusion, ethyl 1-allyl-4-phenyl-piperidine-4-carboxylate is not just a compound with an intriguing formulation, but also a promising subject for ongoing research in chemistry and pharmacology. Its diverse properties and potential applications make it a valuable addition to the chemical literature.

Synonyms
2372-70-5
ISONIPECOTIC ACID, 1-ALLYL-4-PHENYL-, ETHYL ESTER
ethyl 4-phenyl-1-prop-2-enylpiperidine-4-carboxylate
1-Allyl-4-phenylisonipecotic acid ethyl ester
WIN 7681
BRN 0249362
1-Allyl-4-phenyl-4-carbethoxypiperidine
ALLYLNORPETHIDINE
4-22-00-01009 (Beilstein Handbook Reference)
SCHEMBL15735359
DTXSID70178381
Q4733445
Ethyl 4-phenyl-1-(2-propen-1-yl)-4-piperidinecarboxylate
4-Phenyl-1-(2-propen-1-yl)-4-piperidinecarboxylic acid ethyl ester