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Dihydroxylated chalcone

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Identification
Molecular formula
C15H12O4
CAS number
14483-19-3
IUPAC name
1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one
State
State

At room temperature, this compound is usually found in a solid state, often as a powder or crystalline form.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
515.00
Boiling point (Kelvin)
788.15
General information
Molecular weight
272.27g/mol
Molar mass
272.2650g/mol
Density
1.4050g/cm3
Appearence

The compound is typically described as a crystalline solid often exhibiting a yellow to orange coloration.

Comment on solubility

Solubility of 1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one (C15H12O4)

The solubility of 1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one, also known as a flavonoid compound, can be influenced by various factors such as its molecular structure and functional groups. Here are some key points regarding its solubility:

  • Solubility in Water: This compound is expected to have limited solubility in water due to the presence of the hydrophobic phenyl groups, which do not interact favorably with polar water molecules.
  • Solubility in Organic Solvents: It is likely to be more soluble in organic solvents such as ethanol or methanol. This is attributed to the compound's ability to form hydrogen bonds and interactions with organic solvents.
  • pH Dependence: The solubility may vary with changes in pH. The hydroxyl groups (-OH) present in the molecule can be ionized under certain pH conditions, potentially increasing solubility.

In conclusion, while 1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one shows limited solubility in water, its solubility characteristics can change significantly in non-polar organic solvents and at different pH levels. Understanding these factors is crucial in applications where this compound may be used.

Interesting facts

Interesting Facts about 1-(2,4-Dihydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

This fascinating compound, also known as a type of chalcone, exhibits a captivating structure and interesting biological properties that make it a subject of intense research. Chalcones, in general, are known for their role in various biological activities, and this specific compound is no exception. Here are some notable points:

  • Antioxidant Properties: This compound has been noted for its ability to scavenge free radicals, which can contribute to oxidative stress in biological systems. Its antioxidant potential is considered beneficial for health and may play a role in preventing various diseases.
  • Anti-Inflammatory Effects: Research indicates that it may possess anti-inflammatory properties, making it an interesting candidate for therapeutic applications aimed at reducing inflammation in the body.
  • Antimicrobial Activity: Studies have suggested that this compound exhibits inhibitory effects against certain pathogens, hinting at its potential use in developing antimicrobial agents.
  • Phytochemical Significance: Often found in various plants, this compound contributes to the plant’s ecological adaptations and has been utilized in traditional medicine practices across different cultures.
  • Natural Colorants: With its unique structure, compounds like this one are investigated for their utility as natural colorants in the food and cosmetics industries.

As a part of ongoing research, scientists are continually exploring the synthesis and modification of such compounds to enhance their effectiveness or discover new applications. It is a prime example of how a seemingly simple molecule can hold significant promise in the fields of pharmaceuticals and biochemistry.

In the words of chemist Robert H. Grubbs: "The beauty of chemistry lies in its ability to combine simple elements into complex entities with exquisite properties." This compound certainly exemplifies that idea.

Synonyms
GU17;ISL;Isoliquiritigen
Spectrum_000145
SpecPlus_000762
Spectrum2_000875
Spectrum3_001656
Spectrum4_001756
KBioGR_002232
KBioSS_000625
DivK1c_006858
SPBio_000949
CHEMBL3183256
KBio1_001802
KBio2_000625
KBio2_003193
KBio2_005761
KBio3_002631
DTXSID80859558
DXDRHHKMWQZJHT-UHFFFAOYSA-N
HMS3656C17
AKOS030228126
NCGC00090504-10
NS00006266
Q27165761