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Naringenin chalcone

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Identification
Molecular formula
C16H14O4
CAS number
28645-86-3
IUPAC name
2,5-dihydroxy-3-(4-methoxyphenyl)-6-phenyl-cyclohexane-1,4-dione
State
State

At room temperature, Naringenin chalcone is in a solid state, appearing as a yellow crystalline material.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.15
Boiling point (Celsius)
510.00
Boiling point (Kelvin)
783.15
General information
Molecular weight
270.29g/mol
Molar mass
270.2900g/mol
Density
1.2000g/cm3
Appearence

Naringenin chalcone is typically a yellow crystalline powder. It is insoluble in water but soluble in organic solvents, such as ethanol and acetone.

Comment on solubility

Solubility of 2,5-Dihydroxy-3-(4-methoxyphenyl)-6-phenyl-cyclohexane-1,4-dione

The solubility of 2,5-dihydroxy-3-(4-methoxyphenyl)-6-phenyl-cyclohexane-1,4-dione (C16H14O4) is an intriguing topic due to its structural complexity and the influence of functional groups on its solubility traits. Here are a few key considerations:

  • Polar vs. Nonpolar: The presence of two hydroxyl (-OH) groups suggests that this compound has some polar characteristics, potentially enhancing its ability to dissolve in polar solvents like water.
  • Hydrophobic Effects: Conversely, the bulky aromatic rings may contribute to hydrophobic interactions, which could limit solubility in aqueous solutions.
  • Solvent Compatibility: Solubility may be favored in organic solvents (e.g., ethanol, acetone) due to the compound's nonpolar residues, making these solvents suitable for dissolution.
  • Temperature Dependence: Like many organic compounds, solubility may increase with temperature, allowing for increased interactions between solvent molecules and solute.

In conclusion, while the compound may exhibit a degree of solubility in both polar and nonpolar solvents, its actual solubility will depend on the precise conditions, such as temperature and solvent choice. Understanding these nuances is crucial for applications in various chemical processes.

Interesting facts

Exploring 2,5-Dihydroxy-3-(4-methoxyphenyl)-6-phenyl-cyclohexane-1,4-dione

2,5-Dihydroxy-3-(4-methoxyphenyl)-6-phenyl-cyclohexane-1,4-dione is a fascinating compound that presents intriguing properties and potential applications. This compound belongs to a class of organic chemicals that are rich in hydroxyl functional groups, which can profoundly influence their reactivity and biological activities.

Interesting Aspects of the Compound:

  • Aromatic Complexity: The presence of a methoxyphenyl group adds a layer of aromatic character to the compound, enhancing its potential interactions in biological systems.
  • Phenolic Structures: With multiple hydroxyl groups, this compound may exhibit strong antioxidant properties, which can be advantageous in medicinal chemistry by combating oxidative stress.
  • Cyclohexane Core: The cyclohexane ring structure provides a unique three-dimensional shape, which may play a key role in the compound's activity and interaction with biological targets.
  • Potential Uses: Compounds with similar structures have been studied for their potential therapeutic uses, including anti-inflammatory and anti-cancer activities.
  • Natural Occurrence: Structures resembling 2,5-dihydroxy-3-(4-methoxyphenyl)-6-phenyl-cyclohexane-1,4-dione can be found in certain natural products, hinting at the compound's role in nature and its importance in various biochemical pathways.

Overall, the study of 2,5-dihydroxy-3-(4-methoxyphenyl)-6-phenyl-cyclohexane-1,4-dione is significant as it bridges the gap between synthetic chemistry and natural products, highlighting the endless possibilities of organic compounds in pharmaceutical and industrial applications.