Skip to main content

Visnagin

ADVERTISEMENT
Identification
Molecular formula
C16H16O6
CAS number
82-57-5
IUPAC name
4-[(2R)-2,3-dihydroxy-3-methyl-butoxy]furo[3,2-g]chromen-7-one
State
State

Solid at room temperature.

Melting point (Celsius)
104.00
Melting point (Kelvin)
377.15
Boiling point (Celsius)
518.50
Boiling point (Kelvin)
791.70
General information
Molecular weight
310.32g/mol
Molar mass
310.3210g/mol
Density
1.2980g/cm3
Appearence

A white to off-white crystalline powder.

Comment on solubility

Solubility of 4-[(2R)-2,3-dihydroxy-3-methyl-butoxy]furo[3,2-g]chromen-7-one

The solubility of 4-[(2R)-2,3-dihydroxy-3-methyl-butoxy]furo[3,2-g]chromen-7-one in various solvents provides insight into its chemical behavior and potential applications. Understanding solubility can be articulated through several key factors:

  • Polarity: The compound contains both aliphatic and aromatic structures, influencing its overall polarity. This may result in a preference for solubility in polar solvents due to the presence of hydroxyl groups.
  • Solvent Interaction: Common solvents such as water, ethanol, and methanol might exhibit varying degrees of solubility. Typically, the presence of hydroxyl functional groups enhances solubility in alcohols.
  • pH Effect: Changes in pH can significantly alter the solubility of compounds with acidic or basic groups. The mentioned compound, with hydroxyl functionalities, could be affected by the pH of the solvent.
  • Temperature Dependence: Like many organic compounds, solubility may increase with temperature, highlighting the thermal dynamics in solvation processes.

In summary, while empirical studies would provide specific solubility values, the structural characteristics suggest a moderate solubility in polar solvents and a complex interplay between various factors.

Interesting facts

Interesting Facts about 4-[(2R)-2,3-dihydroxy-3-methyl-butoxy]furo[3,2-g]chromen-7-one

This remarkable compound, often categorized under the flavonoid family, is notable for its complex structure and potential pharmacological properties. Some intriguing aspects include:

  • Natural Occurrence: Compounds like this often occur in various plants, contributing to their biological activity and color.
  • Pharmacological Potential: Research suggests that flavonoids can exhibit a wide range of biological activities, including antioxidant, anti-inflammatory, and anticancer properties. This compound may also play a role in modulating enzyme activity and cellular signaling pathways.
  • Synthesis Pathways: The complex synthesis of such molecules often involves multiple steps and can help in understanding reaction mechanisms and the chemistry of flavonoids.
  • Chirality: The presence of a chiral center in the (2R) configuration indicates that this compound can exist in two enantiomeric forms, which could exhibit different biological activities.
  • Influence on Health: Flavonoids have been studied for their impact on human health, particularly their role in reducing the risk of chronic diseases through dietary intake.

Overall, 4-[(2R)-2,3-dihydroxy-3-methyl-butoxy]furo[3,2-g]chromen-7-one exemplifies the richness and diversity of flavonoid compounds, shedding light on their importance in both the plant kingdom and modern medicine.

Synonyms
Oxypeucedanin hydrate
(+)-Oxypeucedanin hydrate
4-[(2R)-2,3-dihydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one
DTXSID90949318
4-((2R)-2,3-dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one
DTXCID201377515
866-277-2
2643-85-8
Prangolarin hydrate
7H-Furo[3,2-g][1]benzopyran-7-one, 4-[(2R)-2,3-dihydroxy-3-methylbutoxy]-
Oxypeucedaninhydrate
(R)-oxypeucedanin hydrate
CHEMBL454060
CHEBI:69829
Aviprin
Prawgol
Hydroxypeucedanin hydrate
(R)-(+)-Oxypeucedanin Hydrate
(+)-Oxypeucedaninhydrate
7H-Furo(3,2-g)(1)benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutoxy)-, (R)-
7H-FURO(3,2-g)(1)BENZOPYRAN-7-ONE, 4-(2,3-DIHYDROXY-3-METHYLBUTOXY)-, (R)-(+)-
MLS000574909
Aviprin (Oxypeucedaninhydrate)
HMS2196F22
HY-N2622
BDBM50361377
MSK164211
AKOS000278024
FO74044
DA-56521
MS-24390
SMR000156244
1ST164211
CS-0023028
NS00094521
Q27138170
4-[(2R)-2,3-dihydroxy-3-methyl-butoxy]furo[3,2-g]chromen-7-one