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Oxprenolol

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Identification
Molecular formula
C15H23NO3
CAS number
6452-71-7
IUPAC name
[2-hydroxy-3-(2-methylphenoxy)propyl] pyridine-3-carboxylate
State
State

Oxprenolol is typically in a solid state at room temperature. It is usually marketed in the form of tablets for medicinal use.

Melting point (Celsius)
146.50
Melting point (Kelvin)
419.65
Boiling point (Celsius)
535.20
Boiling point (Kelvin)
808.35
General information
Molecular weight
265.34g/mol
Molar mass
265.3360g/mol
Density
1.2000g/cm3
Appearence

Oxprenolol is a white or almost white crystalline powder. It may appear as small crystals or a fine powder and does not have any distinct odor.

Comment on solubility

Solubility of [2-hydroxy-3-(2-methylphenoxy)propyl] pyridine-3-carboxylate

The solubility of [2-hydroxy-3-(2-methylphenoxy)propyl] pyridine-3-carboxylate can vary depending on several factors. This compound, featuring both hydrophilic and hydrophobic characteristics, exhibits unique solubility traits:

  • Solvent Dependence: It is generally more soluble in organic solvents compared to water, which is common for many organic compounds.
  • Temperature Influence: Solubility tends to increase with temperature. Heating the solvent can enhance solubility, thus facilitating dissolution.
  • pH Factors: Changes in pH may also affect solubility, especially given the presence of the carboxylate group, which can ionize in more alkaline conditions, potentially increasing solubility in aqueous solutions.

The interplay between the compound's structure and its environment plays a crucial role in its solubility. In summary, it is important to consider the specific conditions under which solubility is evaluated, as they can lead to significant variations in behavior. Remember, solubility is not just about being able to dissolve, but adapting to the medium!

Interesting facts

Exploring [2-hydroxy-3-(2-methylphenoxy)propyl] pyridine-3-carboxylate

[2-hydroxy-3-(2-methylphenoxy)propyl] pyridine-3-carboxylate is a fascinating compound that reflects the complexity and creativity found in modern organic chemistry. This compound belongs to a class of chemicals containing both pyridine and phenoxy groups, making it an intriguing subject for study. Here are some interesting facts that highlight its significance:

  • Structure and Function: The presence of the pyridine ring, a nitrogen-containing heterocyclic structure, imparts unique electronic properties to the compound, allowing for various applications in pharmaceuticals and agrochemicals.
  • Biological Activity: Compounds with similar structures often exhibit diverse biological activities, including antimicrobial and anti-inflammatory properties. This potential for bioactivity makes it a candidate for further pharmacological research.
  • Versatile Synthetic Pathways: The synthesis of this compound can involve multiple approaches, ranging from traditional organic synthesis to more advanced methodologies such as microwave-assisted reactions, highlighting the versatility of modern chemistry techniques.
  • Role in Material Science: Beyond pharmaceuticals, similar derivatives are being explored for their application in materials science, particularly in the development of functional polymers and coatings.
  • Anecdotal Insight: A chemistry professor once stated, “Compounds like [2-hydroxy-3-(2-methylphenoxy)propyl] pyridine-3-carboxylate are the unsung heroes in the drug discovery process—often overlooked, yet pivotal.” Such insights underline the importance of researching small, intricate molecules.

In summary, [2-hydroxy-3-(2-methylphenoxy)propyl] pyridine-3-carboxylate serves as a prime example of how complex organic structures can lead to exciting opportunities in various fields, from medicine to materials science. As research progresses, the potential applications and implications of this compound continue to expand, showcasing the ever-evolving landscape of chemical science.

Synonyms
28060-95-9
DTXSID30950781
2-HYDROXY-3-(2-METHYLPHENOXY)PROPYL PYRIDINE-3-CARBOXYLATE
RefChem:1063350
DTXCID901378926
Mephenesin nicotinate
533-07-3
9490C46O95
3-(o-Tolyloxy)-2-hydroxypropyl-1-nicotinate
UNII-9490C46O95
NICOTINIC ACID, MONOESTER with 3-(o-TOLYLOXY)-1,2-PROPANEDIOL
Q27271660