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4-Phenoxypiperidine

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Identification
Molecular formula
C11H15NO
CAS number
41661-47-6
IUPAC name
4-phenoxypiperidine
State
State

At room temperature, 4-Phenoxypiperidine typically exists as a liquid. Its state can vary slightly with ambient temperature and pressure conditions.

Melting point (Celsius)
-3.70
Melting point (Kelvin)
269.45
Boiling point (Celsius)
287.90
Boiling point (Kelvin)
561.05
General information
Molecular weight
179.24g/mol
Molar mass
179.2440g/mol
Density
1.0530g/cm3
Appearence

4-Phenoxypiperidine is a colorless to pale yellow liquid with a mild odor. It can appear slightly viscous depending on the conditions of storage but is generally clear.

Comment on solubility

Solubility of 4-phenoxypiperidine

4-phenoxypiperidine, with its unique structure, displays interesting solubility characteristics that are noteworthy for its application in various fields. Understanding the solubility of this compound involves considering several factors:

  • Polarity: The presence of the phenoxy group enhances the polarity of the molecule, which typically increases its solubility in polar solvents, such as water.
  • Hydrogen Bonding: The ability of 4-phenoxypiperidine to engage in hydrogen bonding can facilitate its solubility in substances that can act as hydrogen bond donors or acceptors.
  • Alkyl Chains: The piperidine ring contributes to the overall solubility profile. Compounds with alkyl groups generally have better solubility in organic solvents.
  • pH Dependence: The solubility is also influenced by pH levels. At different pH values, the ionization of the compound can significantly alter its solubility in aqueous solutions.

In practice, 4-phenoxypiperidine is more soluble in organic solvents compared to water due to its molecular structure. However, precise solubility values can vary significantly based on the solvent system and environmental conditions. As such, it is always advisable to conduct solubility tests to determine the best medium for application.

Interesting facts

Interesting Facts about 4-Phenoxypiperidine

4-Phenoxypiperidine is a fascinating compound that provides a variety of intriguing insights for both chemists and students of chemistry. This compound is notable due to its unique molecular structure and potential applications in various fields.

Key Features:

  • Structural Highlights: 4-Phenoxypiperidine features a piperidine ring, which is a six-membered nitrogen-containing ring, enabling it to interact in diverse chemical reactions.
  • Pharmacological Potential: This compound is of significant interest in medicinal chemistry, with research indicating its potential as a therapeutic agent. It may exhibit properties useful in the treatment of various neurological disorders.
  • Versatility in Synthesis: 4-Phenoxypiperidine can be synthesized using different methods, making it a valuable starting material for the development of other chemical compounds.
  • Application in Research: It serves as a valuable link in the development of novel molecules, particularly in studies focused on receptor binding and the investigation of central nervous system activity.

As students delve into the study of 4-Phenoxypiperidine, they often emphasize the importance of understanding such compounds to appreciate their role in complex biological systems. The saying, "The beauty of chemistry lies in its infinite possibilities," rings particularly true for multifaceted compounds like this one, which continue to inspire innovation and research.

In summary, 4-Phenoxypiperidine is not just a chemical entity but a gateway to a deeper understanding of both synthetic and medicinal chemistry. The combination of its structural features and prospective applications makes it a compelling subject for further exploration.

Synonyms
4-phenoxypiperidine
3202-33-3
Piperidine, 4-phenoxy-
UNII-AOF4M4L61Z
AOF4M4L61Z
681-811-2
4-Phenoxy-piperidine
MFCD04114971
CHEMBL3904359
4-(phenoxy)piperidine
SCHEMBL211130
KBYPITRKIJKGMD-UHFFFAOYSA-N
ALBB-019283
MFCD0411497
AC5887
BDBM50202730
AKOS000184064
SB36568
PD158979
SY026648
DB-068567
CS-0156070
EN300-49863
10Y-7007
Q27274035