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Cannflavin A

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Identification
Molecular formula
C21H20O5
CAS number
55251-11-3
IUPAC name
3,7,8-trihydroxy-9-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-10-one
State
State

At room temperature, Cannflavin A is a solid.

Melting point (Celsius)
145.50
Melting point (Kelvin)
418.65
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
354.37g/mol
Molar mass
354.3720g/mol
Density
0.0000g/cm3
Appearence

Cannflavin A is generally found as a yellow crystalline solid. It may display varying shades depending on its purity and the presence of other compounds in herbal material.

Comment on solubility

Solubility of 3,7,8-trihydroxy-9-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-10-one

The solubility of the compound C21H20O5, also known as 3,7,8-trihydroxy-9-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-10-one, can be characterized as follows:

  • Solvent Interactions: This compound shows variable solubility depending on the solvent used. Generally, organic solvents such as ethanol and acetone may enhance its solubility due to its polyhydroxylated structure, which can engage in hydrogen bonding.
  • Hydrophilicity vs. Hydrophobicity: The presence of multiple hydroxyl groups suggests a degree of hydrophilicity; however, the large aromatic and aliphatic side chains introduce hydrophobic characteristics, making the compound less soluble in water.
  • Concentration Factors: At lower concentrations, you may observe some degree of solubility in polar solvents, while higher concentrations may lead to precipitation, indicating that solubility is concentration-dependent.

In summary, while 3,7,8-trihydroxy-9-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-10-one displays interesting solubility behaviors, it is essential to consider the effects of solvent choice and concentration for practical applications.

Interesting facts

Interesting Facts about 3,7,8-Trihydroxy-9-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-10-one

This compound, often referred to in the realm of organic and medicinal chemistry, is a fascinating example of a flavonoid structure. Flavonoids are known for their presence in many plants and play numerous roles in plant physiology, including pigmentation and UV filtration. Here's what makes this particular compound intriguing:

  • Bioactivity: This compound has been studied for various potential health benefits, including anti-inflammatory and antioxidant properties. Compounds with similar structures often exhibit activity that supports cardiovascular health and may help mitigate oxidative stress in cells.
  • Structural Complexity: The compound's complex structure features multiple hydroxyl (-OH) groups, contributing to its reactivity and interaction with biological molecules. This complexity can influence its biological activity and pharmacokinetics significantly.
  • Natural Occurrence: Compounds like this one can be found in various plants, particularly in those with medicinal uses. Their natural occurrence often leads chemists to study their extraction and potential applications in traditional medicine.
  • Synthetic Applications: The synthesis of this type of compound provides valuable insights into organic synthesis techniques, showcasing the challenges and innovations in constructing multi-ringed structures essential in pharmaceutical design.
  • Research Potential: Ongoing research is exploring the mechanisms by which this compound exerts its effects, potentially leading to new therapeutic agents that harness the flavonoid class's benefits.

As we explore the chemistry of such compounds, it is essential to remember the significant role they may play in both nature and medicine. The ability to understand and manipulate these compounds can pave the way for innovative treatments and a deeper understanding of biological processes.