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Pirandamine

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Identification
Molecular formula
C25H29NO4
CAS number
026578-66-3
IUPAC name
2-(4-piperidyl)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate
State
State

At room temperature, this compound is typically found in a solid state. It has a stable crystalline form and is handled as a solid under laboratory conditions.

Melting point (Celsius)
221.00
Melting point (Kelvin)
494.15
Boiling point (Celsius)
435.00
Boiling point (Kelvin)
708.15
General information
Molecular weight
431.51g/mol
Molar mass
431.5300g/mol
Density
1.2000g/cm3
Appearence

The compound typically appears as a crystalline solid, often colorless to pale yellow in color. It may also be presented in powder form.

Comment on solubility

Solubility of 2-(4-piperidyl)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate

The solubility of 2-(4-piperidyl)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate can be categorized as follows:

  • In Organic Solvents: This compound typically demonstrates good solubility in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO). This is attributed to the presence of the hydrophobic chromene structure which interacts favorably with nonpolar solvents.
  • In Water: Conversely, the solubility in water is significantly lower due to the large, hydrophobic chromene moiety which restricts hydration. The compound's carboxylate group can form hydrogen bonds, but the overall structure may still render it challenging to dissolve in aqueous environments.

When assessing solubility, it's essential to consider the influence of temperature and pH, which can significantly impact the dissolution process. In general:

  1. Higher temperatures may enhance solubility for many organic compounds.
  2. Altering pH could either increase solubility (through ionization of the carboxylate) or decrease it, dependent on the surrounding media.

In summary, while 2-(4-piperidyl)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate shows favorable solubility in organic solvents, its hydrophobic nature reduces its solubility in water, making it a compound that requires specific conditions for effective dissolution.

Interesting facts

Interesting Facts about 2-(4-piperidyl)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate

The compound 2-(4-piperidyl)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate is a fascinating molecule that merges the realms of organic chemistry and pharmacology. This multi-functional compound has gained attention for its potential applications in medicinal chemistry. Here are some engaging facts about this unique compound:

  • Diversity in Structure: The presence of a chromene moiety in its structure signifies a rich class of compounds known for diverse biological activities. Chromenes are often investigated for their roles in various secondary metabolites.
  • Piperidyl Group: The piperidyl portion provides interesting properties that can enhance binding to biological targets, potentially facilitating interactions with neurotransmitter systems.
  • Biological Activity: Numerous studies suggest that similar compounds can exhibit a range of pharmacological effects, including anti-inflammatory, analgesic, and even anticancer activities.
  • Origin of Chromenes: Chromenes are naturally occurring compounds found in many plants, contributing to their medicinal value and offering sourcing potential for natural product chemistry.
  • Potential Research Directions: This compound's versatility opens up avenues for further research in synthesizing derivatives that may improve efficacy and reduce side effects, making it a candidate for novel drug development.

As researchers delve deeper into the world of 2-(4-piperidyl)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate, their findings may unravel new horizons in therapeutic chemistry. Armed with detailed studies and innovative synthesis techniques, scientists are excited about the potential applications of this compound in treating complex health issues.