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Flavoxate hydrochloride

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Identification
Molecular formula
C24H29ClNO3
CAS number
3717-88-2
IUPAC name
2,3-dimethyl-6-(piperidin-1-ium-1-ylmethyl)chromen-4-one;chloride
State
State

At room temperature, flavoxate hydrochloride is in the solid state, typically presented as a fine powder or crystalline form.

Melting point (Celsius)
173.00
Melting point (Kelvin)
446.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
427.95g/mol
Molar mass
427.0000g/mol
Density
1.2000g/cm3
Appearence

Flavoxate hydrochloride appears as a white to off-white crystalline powder. It is generally odorless and has a bitter taste. The powder is soluble in water and slightly soluble in alcohol.

Comment on solubility

Solubility of 2,3-dimethyl-6-(piperidin-1-ium-1-ylmethyl)chromen-4-one;chloride

The solubility of 2,3-dimethyl-6-(piperidin-1-ium-1-ylmethyl)chromen-4-one;chloride can be characterized by the following key points:

  • Nature of the compound: This compound features both an organic chromenone scaffold and a piperidinium moiety, which influence its solubility profile.
  • Soluble in polar solvents: Due to the presence of the ionic (piperidinium) group, this compound is likely to exhibit good solubility in polar solvents such as water and alcohols.
  • Limited solubility in non-polar solvents: The extensive aromatic structure and the charged group contribute to poor solubility in non-polar environments such as hydrocarbons.
  • pH dependence: The solubility may also be affected by the pH of the solution, as ionic compounds generally have better solubility in acidic to neutral pH levels.

In summary, the solubility of 2,3-dimethyl-6-(piperidin-1-ium-1-ylmethyl)chromen-4-one;chloride is primarily influenced by its ionic characteristics and molecular structure. This compound showcases significant potential for solubility in polar solvents, making it suitable for a variety of applications in aqueous environments.

Interesting facts

Interesting Facts About 2,3-Dimethyl-6-(piperidin-1-ium-1-ylmethyl)chromen-4-one; Chloride

The compound 2,3-dimethyl-6-(piperidin-1-ium-1-ylmethyl)chromen-4-one; chloride is an intriguing member of the chromone family, a class of compounds that display unique biological activities and structural diversity. Here are some notable facts:

  • Structural Complexity: This compound showcases a sophisticated structure that combines a chromone core with a piperidinyl unit. The incorporation of the piperidine moiety can significantly enhance the pharmacological properties of the molecule.
  • Biological Significance: Compounds related to chromones have been studied extensively for their various biological roles, including antioxidant, antimicrobial, and anti-inflammatory activities. The potential therapeutic applications are vast and varied.
  • Versatility in Synthesis: The synthesis of chromones often involves creative synthetic strategies, allowing for the introduction of various substituents at specific positions. This versatility makes them crucial in medicinal chemistry research.
  • Charge Influence: The presence of the piperidinium group introduces a positive charge, which can influence the compound's solubility and interaction with biological systems. This feature frequently leads to increased bioavailability in medicinal contexts.
  • Research Potential: Scientists are continuously exploring the potential of similar compounds in drug discovery, aiming to develop novel therapies targeting diseases such as cancer or neurodegenerative disorders.

Overall, the 2,3-dimethyl-6-(piperidin-1-ium-1-ylmethyl)chromen-4-one; chloride compound demonstrates how chemical diversity can lead to significant biological implications. As research advances, this class of compounds holds promising potential in various fields, ranging from pharmacology to materials science.

Synonyms
2,3-Dimethyl-6-piperidinomethyl-chromone hydrochloride
REC 7-0108
16146-80-8
2,3-Dimetil-6-piperidinometil-cromone-cloridrato [Italian]
2,3-Dimetil-6-piperidinometil-cromone-cloridrato
CHROMONE, 2,3-DIMETHYL-6-PIPERIDINOMETHYL-, MONOHYDROCHLORIDE
4H-1-Benzopyran-4-one, 2,3-dimethyl-6-(1-piperidinylmethyl)-, hydrochloride