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5,8-Dimethoxy-2-methylchromen-4-one

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Identification
Molecular formula
C13H12O4
CAS number
37255-49-3
IUPAC name
5,8-dimethoxy-2-methyl-chromen-4-one
State
State

At room temperature, this compound is generally found as a solid.

Melting point (Celsius)
123.50
Melting point (Kelvin)
396.65
Boiling point (Celsius)
396.30
Boiling point (Kelvin)
669.45
General information
Molecular weight
250.26g/mol
Molar mass
250.2640g/mol
Density
1.2100g/cm3
Appearence

5,8-Dimethoxy-2-methylchromen-4-one is a crystalline solid, typically appearing as a pale yellow to off-white powder.

Comment on solubility

Solubility of 5,8-Dimethoxy-2-methyl-chromen-4-one

5,8-Dimethoxy-2-methyl-chromen-4-one is an interesting compound regarding its solubility characteristics. The following points summarize its solubility profile:

  • Solvent Compatibility: This compound is primarily soluble in organic solvents such as ethanol, methanol, and chloroform, which are common choices for dissolving organic compounds.
  • Water Solubility: While it may have limited solubility in water, it is generally considered insoluble or only slightly soluble due to its hydrophobic structure.
  • Influence of Temperature: Like many organic compounds, solubility can increase with temperature. Thus, heating the solvent may help in enhancing the dissolution process.
  • pH Sensitivity: The solubility can be affected by the pH of the solution, as changes in acidity or basicity can influence the ionization state of the compound.

In conclusion, while 5,8-Dimethoxy-2-methyl-chromen-4-one exhibits good solubility in organic solvents, it may present challenges when attempting to dissolve it in aqueous environments. It is essential to select the appropriate solvent for effective utilization in experimental setups.

Interesting facts

Interesting Facts about 5,8-Dimethoxy-2-methyl-chromen-4-one

5,8-Dimethoxy-2-methyl-chromen-4-one, often referred to as a compound within the flavonoid family, has garnered attention for its unique chemical structure and potential applications. Here are some fascinating aspects:

  • Active Ingredients: This compound is characterized by the presence of two methoxy groups and a methyl group attached to the chromenone structure, contributing to its distinctive biological properties.
  • Biological Activity: Research has suggested that its derivatives may exhibit antioxidant, anticancer, and anti-inflammatory activities, making it a subject of interest in pharmacology and medicinal chemistry.
  • Source: Flavonoids like 5,8-dimethoxy-2-methyl-chromen-4-one are often derived from plants, with many showing potential in traditional medicine practices across various cultures.
  • Research Applications: Scientists study such compounds to explore their efficacy in developing new therapeutic agents, as their molecular structure often influences their interaction with biological targets.
  • Chemical Versatility: The ability to modify groups on the chromenone ring provides a platform for synthetic chemists looking to develop novel compounds with specific properties.

Overall, this compound exemplifies the intricate relationship between chemical structure and biological function, illustrating why compounds from the flavonoid family continue to be a focal point of research in the fields of phytochemistry and drug development.

Synonyms
5,8-Dimethoxy-2-methylchromone
CHROMONE, 5,8-DIMETHOXY-2-METHYL-
5,8-Dimethoxy-2-methyl-4H-1-benzopyran-4-one
HCM42RU6LX
NSC 73723
BRN 0188703
4-Chromanone, 5,8-dimethoxy-2-methyl-
4H-1-Benzopyran-4-one, 5,8-dimethoxy-2-methyl-
UNII-HCM42RU6LX
NSC-73723
DTXSID40221777
5-18-03-00225 (Beilstein Handbook Reference)
2-METHYL-5,8-DIMETHOXYCHROMONE
5,8-DIMETHOXY-2-METHYL-4H-BENZOPYRAN-4-ONE
DTXCID70144268
4H-1-Benzopyran-4-one, 5,8-dimethoxy-2-methyl-(9CI)
684-734-2
7154-68-9
5,8-dimethoxy-2-methyl-4H-chromen-4-one
5,8-dimethoxy-2-methylchromen-4-one
NSC73723
Chromone,8-dimethoxy-2-methyl-
SCHEMBL13978672
AKOS024323267
WLN: T66 BO EVJ C1 GO1 JO1
DA-38202
4H-1-Benzopyran-4-one,8-dimethoxy-2-methyl-