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Scopoletin

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Identification
Molecular formula
C10H8O4
CAS number
92-61-5
IUPAC name
2-hydroxy-6-methoxy-chromen-7-one
State
State

Scopoletin is a solid at room temperature, normally appearing in its crystal form.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
356.90
Boiling point (Kelvin)
630.05
General information
Molecular weight
192.17g/mol
Molar mass
192.1680g/mol
Density
1.4400g/cm3
Appearence

Scotopoletin is a crystalline solid that is typically colorless or exhibits a slight yellow tint. The compound appears in the form of needle-like or platelet crystals.

Comment on solubility

Solubility of 2-hydroxy-6-methoxy-chromen-7-one (C10H8O4)

2-hydroxy-6-methoxy-chromen-7-one, also known as a derivative of flavonoids, exhibits a moderate solubility profile influenced by its molecular structure.

Factors Influencing Solubility:

  • Polarity: The hydroxyl (-OH) and methoxy (-OCH3) groups contribute to the polar nature of the molecule, enhancing its ability to dissolve in polar solvents.
  • Hydrogen Bonding: The presence of multiple hydroxyl groups allows for stronger hydrogen bonding interactions with solvents, which often increases solubility in water.
  • Solvent Type: Generally, 2-hydroxy-6-methoxy-chromen-7-one is more soluble in polar solvents like ethanol and methanol compared to non-polar solvents.

In summary, while this compound's solubility is favorable in polar environments, its solubility can be limited in non-polar solvents. As with many organic compounds, understanding these solubility characteristics is crucial for applications in areas such as pharmaceuticals and biochemistry.

Interesting facts

Exploring 2-hydroxy-6-methoxy-chromen-7-one

2-hydroxy-6-methoxy-chromen-7-one, a fascinating compound in the flavonoid category, is recognized for its intriguing structural features and diverse biological activities. Here are some interesting facts about this compound:

  • Natural Occurrence: This compound is often found in various plants, contributing to their bioactive properties. Its presence is especially significant in medicinal herbs, highlighting its potential health benefits.
  • Flavonoid Family: As a member of the flavonoid class, 2-hydroxy-6-methoxy-chromen-7-one exhibits antioxidant properties, which can help inhibit oxidative stress in biological systems.
  • Biological Activities: Research has shown this compound to possess a variety of biological activities, including anti-inflammatory, anti-cancer, and anti-microbial effects, making it a subject of interest in pharmacological studies.
  • Chemical Modifications: The unique substitution pattern in its structure suggests that small chemical modifications could yield derivatives with enhanced activities or new properties, thus opening avenues for drug development.
  • Historic Use: Historically, compounds in the coumarin family, including 2-hydroxy-6-methoxy-chromen-7-one, have been used in traditional medicine systems worldwide, showcasing a relationship between chemistry and cultural practices.

As scientists delve deeper into the complexities of 2-hydroxy-6-methoxy-chromen-7-one, we’re not just studying a compound—we’re unlocking a world of potential health solutions and understanding the intricate relationships between plants and their chemical constituents.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." The exploration of compounds like 2-hydroxy-6-methoxy-chromen-7-one exemplifies this ethos, driving both inspiration and innovation within the field of chemistry.