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Vorapaxar

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Identification
Molecular formula
C29H33ClN2O4
CAS number
618385-01-6
IUPAC name
4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholin-4-ium;chloride
State
State

At room temperature, Vorapaxar is a solid compound. It remains stable under normal conditions and should be handled with care to avoid inhalation and contact with skin and eyes.

Melting point (Celsius)
137.00
Melting point (Kelvin)
410.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
492.98g/mol
Molar mass
492.9780g/mol
Density
1.2560g/cm3
Appearence

Vorapaxar is generally observed as a crystalline solid, which is typically off-white in color. The solid is often provided in a powdered form for ease of handling and formulation.

Comment on solubility

Solubility of 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholin-4-ium;chloride

The solubility of 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholin-4-ium;chloride can be assessed through several factors that influence its behavior in various solvents. Generally, the solubility of ionic compounds, such as salts, tends to be influenced by the following properties:

  • Polarity: The compound contains a morpholinium group, which enhances its polarity, making it more soluble in polar solvents.
  • Hydration Energy: The presence of the chloride ion contributes to the hydration energy, promoting higher solubility in water.
  • Functional Groups: The isoxazole ring and phenyl group may affect solubility due to potential interactions with solvents, influencing solubility in organic solvents.

In general, 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholin-4-ium;chloride is expected to exhibit:

  • Good solubility in water due to its ionic nature.
  • Varied solubility in organic solvents, potentially dissolving well in polar organic solvents, while being less soluble in nonpolar solvents.

Ultimately, it is important to experiment and measure the solubility of this compound under specific conditions to better understand its solubility profile. As always, the interaction of your solvent with the compound can significantly dictate the outcomes you observe!

Interesting facts

Interesting Facts about 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholin-4-ium; chloride

4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholin-4-ium; chloride is a fascinating compound that showcases the intersection between organic chemistry and pharmacology.

Key Characteristics

  • Morpholine Derivative: This compound is derived from morpholine, a six-membered ring compound known for its versatile applications in medicinal chemistry.
  • Isolated Ion: The presence of the chloride ion indicates its role as a counterion, which can affect the solubility and biological activity of the compound.
  • Phenylisoxazole Feature: The incorporation of the 3-phenylisoxazole moiety adds significant importance, relating to various biological activities, especially in the fields of neurochemistry and antifungal research.

Applications of the Compound

This compound holds potential in several scientific domains:

  • Pharmacological Research: Compounds like this are often investigated for their role in neuroprotection or as novel therapeutic agents.
  • Material Science: The unique structure may contribute to interaction with polymers, adding to the versatility of its applications.
  • Diagnostics: The specific isoxazole structure can be modified for use in imaging technologies or as markers in biochemical assays.

Quotes from the Scientific Community

"Adaptability in chemical structure often brings forth new biotechnological applications." This notion underscores the significance of compounds such as 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholin-4-ium; chloride in pushing the boundaries of scientific inquiry.

Overall, the study and application of this compound underscore the exciting possibilities that arise from modular design in chemistry, inviting further exploration into its functional capabilities and synthetic pathways!

Synonyms
3-Phenyl-5-(1-morpholinoethyl)isoxazole hydrochloride
14716-63-3
ISOXAZOLE, 5-(1-MORPHOLINOETHYL)-3-PHENYL-, HYDROCHLORIDE