Skip to main content

[4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate

ADVERTISEMENT
Identification
Molecular formula
C21H16O8
CAS number
41443-01-6
IUPAC name
[4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate
State
State

At room temperature, [4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate is typically found in a solid state, allowing it to be easily stored and handled in a laboratory setting.

Melting point (Celsius)
185.00
Melting point (Kelvin)
458.20
Boiling point (Celsius)
383.40
Boiling point (Kelvin)
656.50
General information
Molecular weight
386.34g/mol
Molar mass
386.3360g/mol
Density
1.3650g/cm3
Appearence

The compound appears as a beige to brown powder or crystalline solid. It is generally observed in a finely divided form suitable for its applications.

Comment on solubility

Solubility of [4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate

The solubility of [4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate in various solvents is an important aspect to consider for its potential applications in pharmaceuticals and materials science. This compound features a complex structure that may exhibit differential solubility properties. Here are some key points regarding its solubility:

  • Polar Solvents: Due to the presence of acetoxy groups, this compound may show limited solubility in polar solvents like water.
  • Non-Polar Solvents: It could be more soluble in non-polar organic solvents such as toluene or dichloromethane, as they can better accommodate the organic moieties of the molecule.
  • pH Influence: The solubility may also be pH-dependent, with potential variations observed in acidic or basic conditions, affecting the ionization of functional groups.
  • Temperature Effects: As with many organic compounds, solubility is often enhanced at higher temperatures, facilitating dissolution.

In summary, the solubility behavior of [4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate is dictated by its structural attributes and the solvent environment. Understanding these interactions is crucial for optimizing the use of this compound in practical applications.

Interesting facts

Interesting Facts about [4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] Acetate

[4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate, often referred to in scientific circles for its remarkable structure and potential applications, is a fascinating compound that bridges the realms of organic chemistry and medicinal research.

Key Features and Applications

  • Chromone Derivative: This compound belongs to the chromone family, which is known for its wide range of biological activities, including anti-inflammatory, antioxidant, and anticancer properties.
  • Functional Groups: The presence of multiple acetoxy groups enhances its solubility and reactivity, making it useful in various synthetic and medicinal chemistry applications.
  • Bioactivity: Researchers are exploring several pharmacological effects, with studies indicating potential efficacy in treating various diseases, particularly due to its structural analogs.

Research and Development

The increasing interest in [4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate is often driven by:

  • Exploration of its cytotoxic effects on cancer cells, presenting avenues for targeted therapies.
  • Investigations into its role as an antioxidant, which could contribute to health maintenance and disease prevention.
  • The potential for development into a pharmaceutical agent, showcasing its versatility in drug design.

As noted in various studies, *"The structural diversity offered by chromones opens new frontiers in pharmaceutical chemistry.”* This statement encapsulates the significance of such compounds in contemporary science. There is still much to uncover about [4-(5,7-diacetoxy-4-oxo-chromen-2-yl)phenyl] acetate, making it an exciting focal point of ongoing chemical research.

Synonyms
Apigenin triacetate
3316-46-9
APIGENINTRIACETATE
Triacetyl apigenin
[4-(5,7-diacetyloxy-4-oxochromen-2-yl)phenyl] acetate
6LQX84KDOB
FLAVONE, 4',5,7-TRIHYDROXY-, TRIACETATE
4',5,7-Triacetoxyflavone
2-(4-Acetoxyphenyl)-4-oxo-4H-chromene-5,7-diyl diacetate
4',5,7-Triacetoxy flavone
UNII-6LQX84KDOB
TRIACETYLAPIGENIN
Spectrum2_000291
Spectrum3_001883
4H-1-Benzopyran-4-one, 5,7-bis(acetyloxy)-2-(4-acetyloxy)phenyl-
4a?5,7-Triacetoxyflavone
BSPBio_003386
SPBio_000222
SCHEMBL1676023
CHEMBL3039042
CHEBI:92205
KBio3_002889
DTXSID70186805
IVXFOQQPPONQTB-UHFFFAOYSA-N
4H-1-Benzopyran-4-one, 5,7-bis(acetyloxy)-2-[4-(acetyloxy)phenyl]-
CCG-39849
HY-W748594
SDCCGMLS-0066423.P001
NCGC00178101-01
DA-49686
CS-0793395
G90782
BRD-K12057390-001-01-7
Q27163976
5-(Acetyloxy)-2-[4-(acetyloxy)phenyl]-4-oxo-4H-chromen-7-yl acetate #