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7-Methoxy-5-methyl-2-phenylchromen-4-one

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Identification
Molecular formula
C17H14O3
CAS number
528-48-3
IUPAC name
7-methoxy-5-methyl-2-phenyl-chromen-4-one
State
State

At room temperature, 7-Methoxy-5-methyl-2-phenylchromen-4-one is in a solid state. It exists as a crystalline substance and is often utilized in this form for various chemical applications.

Melting point (Celsius)
167.50
Melting point (Kelvin)
440.60
Boiling point (Celsius)
467.20
Boiling point (Kelvin)
740.40
General information
Molecular weight
282.31g/mol
Molar mass
282.3080g/mol
Density
1.1653g/cm3
Appearence

7-Methoxy-5-methyl-2-phenylchromen-4-one typically appears as a crystalline solid under standard conditions. It can have a yellowish to beige hue, depending on its purity and form. The compound is often available as fine powdery crystals.

Comment on solubility

Solubility of 7-methoxy-5-methyl-2-phenyl-chromen-4-one (C17H14O3)

The solubility of 7-methoxy-5-methyl-2-phenyl-chromen-4-one, a flavonoid derivative, can be quite fascinating. Generally, this compound exhibits a moderate solubility in organic solvents while showing limited solubility in water. Here are some important points regarding its solubility:

  • Polar Solvents: The presence of the methoxy group allows for some interaction with polar solvents, although solubility is still not high.
  • Non-Polar Solvents: The aromatic components and hydrophobic phenyl groups contribute to better solubility in non-polar organic solvents like hexane or chloroform.
  • Temperature Effect: Like many organic compounds, solubility can be affected by temperature; generally, an increase in temperature can enhance solubility in organic solvents.
  • pH Influence: The solubility may vary with pH changes, with potential increases in solubility in acidic or basic conditions due to the ionization of functional groups.

In summary, while 7-methoxy-5-methyl-2-phenyl-chromen-4-one has limited water solubility, its interactions with various organic solvents make it versatile in different chemical environments. Understanding these solubility characteristics is crucial for its applications in fields such as pharmaceuticals and material science.

Interesting facts

Interesting Facts about 7-Methoxy-5-methyl-2-phenyl-chromen-4-one

7-Methoxy-5-methyl-2-phenyl-chromen-4-one, often recognized as a compound belonging to the flavonoid family, possesses remarkable characteristics and applications that scientists find intriguing. Here are some key points to consider:

  • Origin of the Name: The name reflects its structural components; the "chromen" backbone indicates its classification in the flavonoid group, while "7-methoxy" and "5-methyl" highlight specific functional groups that contribute to its activity.
  • Natural Sources: This compound can be found naturally in several plants, particularly in those known for traditional medicinal uses, which have inspired numerous studies on its biological effects.
  • Biological Activity: Research has shown that flavonoids, including this compound, exhibit a range of bioactivities such as antioxidant, anti-inflammatory, and antimicrobial properties. Evidence suggests that compounds like 7-methoxy-5-methyl-2-phenyl-chromen-4-one may play a role in promoting health and preventing diseases.
  • Research Potential: Given its diverse biological effects, this compound is viewed as a potential candidate for drug development. Studies are ongoing to explore its efficacy in areas such as cancer treatment, cardiovascular health, and neuroprotection.
  • Chemical Reactions: The unique structure allows for interesting chemical reactivity, making it a valuable compound for synthetic chemists aiming to create analogs or derive new compounds with enhanced properties.

In conclusion, 7-methoxy-5-methyl-2-phenyl-chromen-4-one is not just an ordinary compound; it is a fascinating example of nature's complexity that continues to inspire scientific inquiry and discovery. As the phrase goes, "Exploration is the engine that drives innovation," and this compound is a key player in the pursuit of new therapeutic discoveries.

Synonyms
methoxyvone
7-methoxy-5-methyl-2-phenylchromen-4-one
Spectrum_000014
Spectrum2_000056
Spectrum3_001778
Spectrum4_000130
Spectrum5_000894
BSPBio_003275
KBioGR_000520
KBioSS_000354
DivK1c_000643
SPECTRUM1400666
SPBio_000211
SCHEMBL3409370
CHEMBL1591080
HMS502A05
KBio1_000643
KBio2_000354
KBio2_002922
KBio2_005490
KBio3_002776
CHEBI:114181
JETSDIPTVSZMLI-UHFFFAOYSA-N
NINDS_000643
CCG-39990
IDI1_000643
NCGC00095871-01
NCGC00095871-02
NCGC00178171-01
7-methoxy-5-methyl-2-phenyl-1-benzopyran-4-one
BRD-K56057104-001-02-9
BRD-K56057104-001-03-7
Q27195222