Skip to main content

Clopidol

ADVERTISEMENT
Identification
Molecular formula
C13H16ClNO2
CAS number
2971-90-5
IUPAC name
3-(4-chlorophenyl)-5-(piperidin-1-ium-1-ylmethyl)isoxazole;chloride
State
State

At room temperature, Clopidol is in a solid state, specifically as a crystalline powder.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
352.25g/mol
Molar mass
352.2510g/mol
Density
1.4100g/cm3
Appearence

Clopidol appears as a solid substance that can vary in color from white to off-white. Its crystalline nature is typical of many organic compounds, giving it a powdery texture.

Comment on solubility

Solubility of 3-(4-chlorophenyl)-5-(piperidin-1-ium-1-ylmethyl)isoxazole;chloride

The solubility of 3-(4-chlorophenyl)-5-(piperidin-1-ium-1-ylmethyl)isoxazole;chloride can be influenced by its structure, particularly due to the presence of ionic and polar functional groups. In general, the solubility of a compound can be assessed through several key factors:

  • Ionic Nature: The presence of the +1 piperidinium ion suggests a tendency for solubility in polar solvents, especially in water.
  • Hydrophobic Character: The 4-chlorophenyl group may contribute to hydrophobic interactions, potentially decreasing solubility in aqueous solutions.
  • Interactions with Solvents: Ionic compounds typically exhibit enhanced solubility in polar solvents compared to non-polar solvents.

In conclusion, while the chloride salt form of 3-(4-chlorophenyl)-5-(piperidin-1-ium-1-ylmethyl)isoxazole suggests a favorable solubility profile in polar environments, the overall solubility will depend on the balance between its ionic characteristics and the hydrophobic influence of the aromatic ring. As the saying goes, "Like dissolves like", emphasizing the importance of matching solubility behavior with the proper solvent conditions.

Interesting facts

Interesting Facts about 3-(4-chlorophenyl)-5-(piperidin-1-ium-1-ylmethyl)isoxazole;chloride

This fascinating compound features a unique structure that combines the isoxazole ring with a piperidine moiety, creating intriguing possibilities for its applications in medicinal chemistry. The presence of the chlorophenyl group enhances its potential pharmacological properties, making it a candidate for various biological activities.

Key Highlights:

  • Diverse Applications: Compounds similar to this one have been explored for their potential in treating neurological disorders, showcasing the importance of their structural components in medicinal efficacy.
  • Ionization: The piperidine moiety in its ionic form may contribute to increased solubility in biological systems, which is an essential characteristic for drug delivery.
  • Antimicrobial Potential: Related isoxazole derivatives have exhibited antimicrobial and antifungal properties, making them valuable in pharmaceutical research for developing new antibiotics.
  • Research Interest: Ongoing studies are focused on understanding the mechanisms of action for compounds like this, which could lead to breakthroughs in therapeutic strategies.

As researchers continue to investigate the implications of this compound, they emphasize the importance of structural modifications in designing more effective therapeutic agents. As a student of chemistry, it’s exciting to consider how variations in molecular structure can lead to vastly different biological activities and applications.

In the words of chemist Lord Kelvin, “If you can’t measure it, you can’t improve it.” This sentiment rings true in the study of compounds like this, where understanding precise molecular interactions can lead to significant advancements in science and medicine.

Synonyms
3-(p-Chlorophenyl)-5-(piperidinomethyl)isoxazole hydrochloride
5500-11-8
ISOXAZOLE, 3-(p-CHLOROPHENYL)-5-(PIPERIDINOMETHYL)-, HYDROCHLORIDE