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Norwogonin

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Identification
Molecular formula
C16H12O4
CAS number
491-70-3
IUPAC name
5-hydroxy-7-methoxy-2-methyl-chromen-4-one
State
State

At room temperature, Norwogonin is a solid. It is typically stable under normal conditions.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
476.50
Boiling point (Kelvin)
749.65
General information
Molecular weight
270.27g/mol
Molar mass
270.2410g/mol
Density
1.3830g/cm3
Appearence

Norwogonin is a yellow crystalline solid. It often appears as needle-like structures when observed under a microscope.

Comment on solubility

Solubility of 5-hydroxy-7-methoxy-2-methyl-chromen-4-one

5-hydroxy-7-methoxy-2-methyl-chromen-4-one, commonly known as flavonoid compounds, exhibits interesting solubility characteristics that are essential for its biological activity and applications. Here are some key points regarding its solubility:

  • Polarity: The presence of hydroxyl (-OH) and methoxy (-OCH3) groups contributes to both polar and non-polar properties, allowing for varying solubility in different solvents.
  • Solvent Compatibility: Generally, this compound can dissolve effectively in organic solvents such as ethanol, methanol, and acetone, but may possess limited solubility in water.
  • Temperature Dependence: Solubility can be influenced by temperature, where higher temperatures typically improve solubility in organic solvents.
  • pH Influence: The solubility tends to increase in more alkaline solutions due to the ionization of the hydroxyl groups.

In summary, understanding the solubility of 5-hydroxy-7-methoxy-2-methyl-chromen-4-one is crucial, considering its potential applications in pharmaceuticals and nutrition. It serves as a reminder of how chemical structure directly influences solubility behavior.

Interesting facts

5-Hydroxy-7-methoxy-2-methyl-chromen-4-one: An Intriguing Compound

This compound is a member of the flavonoid family, renowned for its wide array of biological activities and health benefits. Flavonoids, such as 5-hydroxy-7-methoxy-2-methyl-chromen-4-one, are widely studied for their potential in pharmaceutical applications and their role as antioxidants. Here are some fascinating insights:

  • Natural Antioxidant: Compounds from this class have demonstrated remarkable antioxidant properties, helping to combat oxidative stress in cells.
  • Anti-inflammatory Effects: Research indicates that flavonoids can help reduce inflammation, making them a focal point in studies aimed at developing anti-inflammatory drugs.
  • Plant Origin: This specific compound can often be derived from various plants, notably those in traditional medicine, hinting at its historical use in herbal remedies.
  • Potential Health Benefits: Multiple studies suggest that flavonoids may reduce the risk of chronic diseases, such as heart disease and certain types of cancer.
  • Biological Activity: The properties of the compound can vary significantly, depending on its structure and the nature of the substituents on the chromen backbone.

In the realm of pharmacognosy, this compound exemplifies the intersection of chemistry and nature, where scientists continue to draw inspiration from natural products for drug development. As a chemistry student, one might find that delving into the synthesis and applications of such compounds can enhance not only one's understanding of organic chemistry but also its practical implications in health sciences.

In conclusion, exploring 5-hydroxy-7-methoxy-2-methyl-chromen-4-one provides a valuable insight into both the intricate world of flavonoids and the promising avenues they open up in the fields of medicine and health.

Synonyms
Eugenin
5-HYDROXY-7-METHOXY-2-METHYLCHROMONE
5-Hydroxy-7-methoxy-2-methyl-4H-1-benzopyran-4-one
5-hydroxy-7-methoxy-2-methylchromen-4-one
5-Hydroxy-7-methoxy-2-methylchrone
CHEBI:67374
E8D279U89S
4H-1-Benzopyran-4-one, 5-hydroxy-7-methoxy-2-methyl-
Chromone, 5-hydroxy-7-methoxy-2-methyl-
DTXSID80197381
2-Methyl-5-hydroxy-7-methoxychromone
5-Hydroxy-7-methoxy-2-methyl-Chromone
2-METHYL-7-METHOXY-5-HYDROXYCHROMONE
DTXCID90119872
sutubqhkzrnzra-uhfffaoysa-n
480-34-2
5-Hydroxy-7-methoxy-2-methyl-4H-chromen-4-one
CHEMBL446974
MFCD03001454
UNII-E8D279U89S
SCHEMBL1860860
CS-D0395
BDBM50338662
AKOS022506034
AS-30953
DA-73247
HY-33351
C20210
AN-970/40920732
5-Hydroxy-7-methoxy-2-methyl-4H-chromen-4-one #
Q5408256