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Genistein

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Identification
Molecular formula
C15H10O5
CAS number
446-72-0
IUPAC name
8-[2-(dimethylamino)ethoxy]-3-(4-methoxyphenyl)-2-methyl-chromen-4-one
State
State

Genistein is typically found to be in a solid state at room temperature.

Melting point (Celsius)
297.00
Melting point (Kelvin)
570.15
Boiling point (Celsius)
545.60
Boiling point (Kelvin)
818.80
General information
Molecular weight
270.25g/mol
Molar mass
270.2470g/mol
Density
1.3800g/cm3
Appearence

It appears as a yellowish crystalline powder.

Comment on solubility

Solubility of 8-[2-(dimethylamino)ethoxy]-3-(4-methoxyphenyl)-2-methyl-chromen-4-one

The solubility of 8-[2-(dimethylamino)ethoxy]-3-(4-methoxyphenyl)-2-methyl-chromen-4-one can be highly dependent on various factors, mainly due to its complex structure. Understanding its solubility is crucial for its application in different fields, particularly in pharmaceuticals and chemical research.

Key Factors Influencing Solubility:

  • Polarity: The presence of polar functional groups, like the dimethylamino and ethoxy groups, can enhance solubility in polar solvents.
  • Hydrogen Bonding: The potential for hydrogen bonding within the molecule or with solvents can significantly affect solubility, making it more soluble in alcohols and other protic solvents.
  • Temperature: As with many compounds, an increase in temperature generally leads to higher solubility.
  • pH Level: The solubility may also vary with pH, especially since the dimethylamino group can be protonated under acidic conditions, potentially increasing the solubility in polar solvents.

To summarize, the solubility of 8-[2-(dimethylamino)ethoxy]-3-(4-methoxyphenyl)-2-methyl-chromen-4-one can be broadly characterized as:

  • More soluble in polar solvents
  • Less soluble in non-polar solvents

In conclusion, when working with this compound, it is essential to consider these factors for optimal use and application. As stated, "The nature of solubility is intricately linked to molecular structure and environmental conditions."

Interesting facts

Interesting Facts about 8-[2-(dimethylamino)ethoxy]-3-(4-methoxyphenyl)-2-methyl-chromen-4-one

This compound, known as a chromenone derivative, exhibits a fascinating profile of biological activity and potential applications. As a member of the flavonoid family, its structure allows it to interact with a variety of biological systems. Here are some compelling aspects of this compound:

  • Biological Significance: Chromenones are noted for their diverse pharmacological properties, including anti-inflammatory, antioxidant, and anticancer activities. This particular compound may offer unique therapeutic potentials.
  • Synthetic Utility: The presence of the dimethylamino and methoxy groups in its structure suggests that this compound could be valuable in medicinal chemistry for the development of new drug candidates.
  • Structural Diversity: The chromenone scaffold not only contributes to unique biological activities but also serves as a platform for further chemical modifications, which can lead to the discovery of novel compounds.
  • Research Interest: Ongoing studies focus on exploring the mechanisms of action and the potential of such compounds in therapeutic applications, energizing the field of natural product chemistry.
  • Applications in Agriculture: Beyond pharmaceuticals, flavonoid derivatives like this compound can be advantageous in agricultural practices as natural pesticides or growth promoters.

Due to its multifaceted nature, 8-[2-(dimethylamino)ethoxy]-3-(4-methoxyphenyl)-2-methyl-chromen-4-one holds promise for future research and applications, making it a compound of considerable interest within chemical and biomedical sciences.

Synonyms
13004-41-6
ISOFLAVONE, 7-(2-(DIMETHYLAMINO)ETHOXY)-4'-METHOXY-2-METHYL-
8-[2-(dimethylamino)ethoxy]-3-(4-methoxyphenyl)-2-methylchromen-4-one
BRN 1262259
7-(2-(Dimethylamino)ethoxy)-4'-methoxy-2-methylisoflavone
DTXSID40156318