Skip to main content

Visnagin

ADVERTISEMENT
Identification
Molecular formula
C13H10O4
CAS number
82-57-5
IUPAC name
(2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one
State
State

At room temperature, Visnagin is typically a solid. It presents itself as crystalline in form, stable under standard atmospheric conditions, making it suitable for handling in laboratory settings without complex containment.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
457.00
Boiling point (Kelvin)
730.15
General information
Molecular weight
260.27g/mol
Molar mass
260.2720g/mol
Density
1.2120g/cm3
Appearence

Visnagin appears as a colorless crystalline solid. It is often isolated from natural sources in its crystalline form and tends to exhibit a transparent or translucent appearance when adequately purified. The crystalline structure can vary slightly, leading to different shades of white or occasionally a faint tinge if impurities are present.

Comment on solubility

Solubility of (2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one

The solubility of the compound (2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one can be quite multifaceted due to its unique chemical structure. Understanding its solubility properties is essential for applications in medicinal chemistry and the formulation of bioactive compounds.

Key factors influencing the solubility of this compound include:

  • Polarity: The presence of functional groups such as hydroxyl (–OH) can enhance solubility in polar solvents. However, its extensive ring structure may limit interactions with water.
  • Temperature: Increasing temperature generally enhances solubility for many organic compounds by providing energy to overcome lattice energies.
  • pH Level: The ionization state of the hydroxyl group may vary with pH, further influencing aqueous solubility.
  • Solvent Choice: While the compound might exhibit limited solubility in water, it is often more soluble in organic solvents such as ethanol or dimethyl sulfoxide (DMSO).

In conclusion, the solubility profile of (2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one presents a diverse landscape influenced by its molecular architecture and external conditions. As such, it serves as a compelling subject for further exploration in solubility science.

Interesting facts

Interesting Facts about (2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one

This compound, with its complex name, is a fascinating example of a chromenone derivative. Here are some intriguing aspects that showcase its unique characteristics and potential applications:

  • Structural Diversity: The compound features a hydrofurochromenone structure, which is notable for its multiple functional groups, including a hydroxyl group. This contributes to its potential reactivity and versatility in chemical synthesis.
  • Biological Significance: Compounds like this one are believed to possess various biological activities, including antioxidant and anti-inflammatory properties. Researchers often explore these characteristics for potential therapeutic applications in medicine.
  • Natural Occurrence: Many similar compounds are found in plant species, indicating a possible role in plant defense mechanisms. They may act as secondary metabolites, offering protection against herbivores or pathogens.
  • Synthetic Applications: The intricate structure lends itself well to organic synthesis, allowing chemists to create derivatives that might possess enhanced or altered properties. These derivatives can be studied for new pharmacological activities.
  • Research Potential: This compound is of great interest in the field of natural products chemistry, where scientists investigate its structure-activity relationships. Such studies could lead to the discovery of novel compounds with useful biological effects.

In summary, the (2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one stands as a testament to the rich diversity of chemical compounds. Its multifaceted structure and potential applications continue to intrigue scientists and researchers, opening doors to further exploration in both chemistry and biology.

Synonyms
Nodakenetin
495-32-9
(-)-Marmesin
Prangeferol
PKL4EW8LPQ
NODAKATIN
CHEBI:132623
(R)-2-(1-Hydroxy-1-methylethyl)-2,3-dihydro-7H-furo(3,2-g)(1)benzopyran-7-one
(2R)-2-(1-hydroxy-1-methylethyl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one
(2R)-2-(1-hydroxy-1-methylethyl)-2,3-dihydro-7H-furo(3,2-g)chromen-7-one
GlyTouCan:G75458TV
G75458TV
Nodakenitin
(2R)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one
(R)-2-(2-Hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one
Nodakenetic
NANI
UNII-PKL4EW8LPQ
MLS001163827
orb1301290
(R)-(-)-NODAKENETIN
CHEMBL1464240
SCHEMBL29471037
CHEBI:49083
DTXSID00964239
HMS2871G16
HY-N2276
s3245
(2R)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-g]chromen-7-one
AKOS016023681
AC-35120
DA-56239
MS-23485
SMR000539229
CS-0019605
C09278
Q27121472
2-(2-Hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one
(R,S)-2-(1-Hydroxy-1-methyl-ethyl)-2,3-dihydro-furo[3,2-g]chromen-7-one
7H-Furo(3,2-g)(1)benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (R)-
7H-FURO(3,2-G)(1)BENZOPYRAN-7-ONE, 2,3-DIHYDRO-2-(1-HYDROXY-1-METHYLETHYL)-, (-)-
7H-FURO(3,2-G)(1)BENZOPYRAN-7-ONE, 2,3-DIHYDRO-2-(1-HYDROXY-1-METHYLETHYL)-, (2R)-
7H-Furo[3,2g][1]-benzopyran-7-one, (-2,3-dihydro-2-(1-hydroxy-1-hydroxymethylethyl)-, (R)