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Etoxadrol

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Identification
Molecular formula
C18H27NO2
CAS number
31626-01-2
IUPAC name
(1,3-dimethyl-4-phenyl-4-piperidyl) propanoate
State
State

At room temperature, Etoxadrol is usually in the form of a solid crystalline powder.

Melting point (Celsius)
63.50
Melting point (Kelvin)
336.65
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
289.42g/mol
Molar mass
289.4090g/mol
Density
1.0654g/cm3
Appearence

Etoxadrol typically appears as a white or off-white crystalline powder.

Comment on solubility

Solubility of (1,3-dimethyl-4-phenyl-4-piperidyl) propanoate

The solubility of (1,3-dimethyl-4-phenyl-4-piperidyl) propanoate can be influenced by a variety of factors, including its molecular structure and the surrounding environment. Understanding the solubility properties of this compound is essential for various applications. Here are some key points to consider:

  • Solvent Polarity: The solubility largely depends on the polarity of the solvent used. Non-polar solvents often dissolve non-polar substances, while polar solvents are effective for polar compounds.
  • Temperature Effects: An increase in temperature typically increases solubility. As the kinetic energy of the molecules increases, more solute can dissolve.
  • pH Levels: The solubility can also change with varying pH levels. Compounds with basic or acidic functional groups may become more soluble in corresponding solutions.
  • Hydrogen Bonding: The presence of hydrogen bond donors and acceptors in the compound can significantly affect its solubility. Compounds capable of forming hydrogen bonds with water are generally more soluble.

In conclusion, understanding the solubility of (1,3-dimethyl-4-phenyl-4-piperidyl) propanoate requires considering these factors, as they interact to define how well the compound can be dispersed in various solvents. Such knowledge is crucial for its applications in pharmaceuticals, organic synthesis, and other chemical processes.

Interesting facts

Interesting Facts about (1,3-Dimethyl-4-phenyl-4-piperidyl) Propanoate

(1,3-Dimethyl-4-phenyl-4-piperidyl) propanoate is a fascinating compound with a noteworthy role in organic chemistry and drug development. This compound features a piperidine ring, which is a key structure in many important biologically active molecules.

Key Characteristics

  • Diverse Applications: This compound is often used in research as a precursor for synthesizing other pharmaceutical agents.
  • Bioactivity: The piperidine ring contributes to its potential neuroactive properties, making it interesting for studies related to brain chemistry.
  • Synthetic Utility: The presence of dimethyl and phenyl groups enhances the compound's reactivity and stability during chemical reactions.

Structure-Activity Relationship

The structure of (1,3-dimethyl-4-phenyl-4-piperidyl) propanoate provides valuable insight into its biological activity:

  • The dimethyl groups often enhance solubility, allowing for better interaction in biological systems.
  • The phenyl substituent contributes to its lipophilicity, which can facilitate the passage through biological membranes.

Quote

As scientists explore the relationship between structure and function, compounds like (1,3-dimethyl-4-phenyl-4-piperidyl) propanoate serve as vital tools in understanding complex biological processes. The piperidine framework, in particular, remains a cornerstone in medicinal chemistry.

In summary, (1,3-dimethyl-4-phenyl-4-piperidyl) propanoate exemplifies the intersection of chemical structure and biological activity, providing a rich area for further exploration and discovery in pharmaceutical research.

Synonyms
ALPHAPRODINE
Prodine
(1,3-dimethyl-4-phenylpiperidin-4-yl) propanoate
77-20-3
1,3-dimethyl-4-phenylpiperidin-4-yl propanoate
NCGC00168347-01
ChemDiv1_023028
Oprea1_010034
Oprea1_576081
SCHEMBL25054
CHEMBL1623765
HMS652G16
DTXSID70859103
STK676786
AKOS000601516
NCGC00168347-02
NS00015666
AB00275603-07
Q4346433
Q18002830