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Pentaacetylgenistein

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Identification
Molecular formula
C31H24O13
CAS number
125345-43-9
IUPAC name
[3,5-diacetoxy-4-oxo-2-(3,4,5-triacetoxyphenyl)chromen-7-yl] acetate
State
State

At room temperature, Pentaacetylgenistein is a solid. It is stable under standard conditions but should be stored away from moisture and light to prevent degradation.

Melting point (Celsius)
122.00
Melting point (Kelvin)
395.15
Boiling point (Celsius)
615.70
Boiling point (Kelvin)
888.90
General information
Molecular weight
552.51g/mol
Molar mass
552.5110g/mol
Density
1.4600g/cm3
Appearence

Pentaacetylgenistein typically appears as a white to off-white crystalline powder. The compound is usually purified for chemical research or industrial use.

Comment on solubility

Solubility of [3,5-diacetoxy-4-oxo-2-(3,4,5-triacetoxyphenyl)chromen-7-yl] acetate

The solubility of the compound [3,5-diacetoxy-4-oxo-2-(3,4,5-triacetoxyphenyl)chromen-7-yl] acetate can be quite intricate due to its complex structure and acetoxy groups. Understanding its solubility characteristics can be pivotal in various applications.

Factors Influencing Solubility:

  • Polarity: The presence of multiple acetoxy groups suggests a potential for increased polarity, which can enhance solubility in polar solvents.
  • Hydrogen Bonding: The acetoxy groups may engage in hydrogen bonding with solvents, further affecting solubility.
  • Molecular Interactions: The chromen-7-yl core's interactions with different solvents, including the potential for π-π stacking, can also play a role.

In general:

  • The compound may exhibit good solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO).
  • Its solubility in water may be limited due to the bulky chromenyl structure, though the acetoxy groups might offer some level of interaction with aquatic environments.

Considering these factors, it is essential to assess the solubility experimentally under various conditions to gain a comprehensive understanding of how this compound behaves in different environments. Quotes from literature often highlight the nuanced nature of solubility, stating that, "The solubility is greatly influenced by both molecular structure and environmental parameters." Thus, accurate assessments are critical for effective application and utilization.

Interesting facts

Interesting Facts about [3,5-diacetoxy-4-oxo-2-(3,4,5-triacetoxyphenyl)chromen-7-yl] acetate

This compound belongs to the class of flavonoids, a diverse group of phytonutrients that are renowned for their antioxidants and anti-inflammatory properties. Flavonoids are often responsible for the vibrant colors found in fruits and flowers, contributing not only to aesthetic appeal but also to health benefits.

  • Health Benefits: Many studies have suggested that flavonoids can promote cardiovascular health. They may help improve blood circulation and reduce cholesterol levels.
  • Natural Sources: Compounds similar to this one can be naturally sourced from various plants, particularly fruits like apples, berries, and grapes. The presence of acetoxy groups in this compound suggests a close relationship to plant-derived secondary metabolites.
  • Potential Applications: Given its structural components, this compound might also find its way into pharmaceuticals due to its potential anti-cancer and neuroprotective properties. Research into flavonoids has highlighted their role in combating oxidative stress.
  • Antimicrobial Activity: Many flavonoids exhibit antimicrobial properties, making them potential candidates for developing natural preservatives in food systems or new antimicrobial agents in medicine.

As a scientist studying this compound, one can appreciate its intricate structure and the potential implications it may hold not only in the field of health sciences but also in agriculture and nutrition. As we explore the diverse applications of flavonoids, understanding compounds like [3,5-diacetoxy-4-oxo-2-(3,4,5-triacetoxyphenyl)chromen-7-yl] acetate furthers our grasp of nature’s chemistry.

In the words of renowned chemist Sir Derek Barton, “There is no more exciting area of chemistry than that of the interaction of molecules with one another, and there is no more vital sphere of applied research than that of drug design.” This compound exemplifies the intersection of fundamental science and practical application.

Synonyms
Myricetin hexaacetate
14813-29-7
MYRICETINHEXAACETATE
[3,5-diacetyloxy-4-oxo-2-(3,4,5-triacetyloxyphenyl)chromen-7-yl] acetate
BRN 0381787
3,3',4',5,5',7-Hexahydroxyflavone hexaacetate
4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-, hexaacetate
CHEMBL480305
SCHEMBL20581611
DTXSID60163887
FLAVONE, 3,3',4',5,5',7-HEXAHYDROXY-, HEXAACETATE
4H-1-Benzopyran-4-one, 3,5,7-tris(acetyloxy)-2-(3,4,5-tris(acetyloxy)phenyl)-