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Resveratrol

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Identification
Molecular formula
C14H12O3
CAS number
501-36-0
IUPAC name
5-[2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol
State
State

Under standard conditions, resveratrol is a solid. It is often found in a crystalline form and can be extracted and isolated from certain plant sources.

Melting point (Celsius)
261.00
Melting point (Kelvin)
534.15
Boiling point (Celsius)
449.00
Boiling point (Kelvin)
722.15
General information
Molecular weight
228.25g/mol
Molar mass
228.2470g/mol
Density
1.5383g/cm3
Appearence

Resveratrol typically appears as an off-white to yellowish crystalline solid. It may also be available in the form of a powder for certain applications.

Comment on solubility

Solubility of 5-[2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol (C14H12O3)

The solubility of 5-[2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol can be quite interesting to explore due to its unique chemical structure and the presence of multiple functional groups. This compound, often referred to as a form of bisphenol or phenolic compound, exhibits characteristic solubility behavior influenced by its hydroxyl (-OH) groups.

Factors Influencing Solubility:

  • Hydroxyl Groups: The presence of two hydroxyl groups enhances solubility in polar solvents like water.
  • Hydrophobic Interactions: The benzene rings contribute hydrophobic segments, which can impact solubility in non-polar solvents.
  • pH Dependence: Solubility may vary with changes in pH, as ionization of the hydroxyl groups can be affected by the environment.

Furthermore, solvent interactions are vital. The amphiphilic nature of this compound may lead to nuanced solubility profiles, encouraging exploration in both:

  • Water: Likely to be moderately soluble due to hydrogen bonding.
  • Organic solvents: May exhibit lower solubility levels depending on the solvent's polarity.

Consequently, when discussing the solubility of C14H12O3, it becomes crucial to consider the balance between hydrophilic and hydrophobic structures, influencing how and where it can dissolve.

Interesting facts

Exploring 5-[2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol

5-[2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol is a fascinating compound that captures the interest of chemists and biochemists alike. This compound, often associated with the class of polyphenols, exhibits a rich tapestry of functionalities that make it noteworthy in various fields of research.

Key Characteristics

  • Antioxidant Properties: This compound is recognized for its potential antioxidant activities. Antioxidants are essential in combating oxidative stress, and polyphenolic compounds like this one play a significant role in health.
  • Potential Health Benefits: Studies suggest that compounds similar to this might contribute to cardiovascular health, neuroprotection, and anti-inflammatory effects, making them of great interest in medical research.
  • Synthetic Routes: The synthesis of this compound can involve advanced organic techniques, making it an excellent example for students to study synthetic methodologies in organic chemistry.
  • Application in Material Science: With its unique structural features, this compound may find applications in developing functional materials, such as sensors or catalysts, highlighting its versatility.

In the Laboratory

The vibrancy of 5-[2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol extends beyond its chemical properties:

  • Research Utility: It serves as an intriguing subject for students and researchers investigating the relationship between chemical structure and biological activity.
  • Educational Impact: Its synthesis often forms part of advanced organic chemistry curricula, offering insights into mechanisms and reactions.

As one delves deeper into the chemistry of this compound, it becomes clear that it embodies the intersection of chemical innovation and health sciences, marking its significance in the ongoing exploration of bioactive compounds. In the words of renowned chemist Marie Curie, “Nothing in life is to be feared, it is only to be understood.” The journey to understand compounds like this one reveals the beautiful complexity of chemistry that fuels scientific discovery and innovation.

Synonyms
375823-41-9
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-
(resveratrol)
1,3-Benzenediol, 5-[2-(4-hydroxyphenyl)ethenyl]-
Spectrum_001148
SpecPlus_000391
(Cis-Trans)-Resveratrol
Prestwick0_000508
Prestwick1_000508
Spectrum2_001497
Spectrum3_001821
Spectrum4_001896
MolMap_000045
5-[2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol
Oprea1_727238
KBioGR_000454
KBioGR_002457
KBioSS_000454
KBioSS_001628
DivK1c_006487
SPBio_001513
SPBio_002356
CHEMBL2019155
KBio1_001431
KBio2_000454
KBio2_001628
KBio2_003022
KBio2_004196
KBio2_005590
KBio2_006764
KBio3_000847
KBio3_000848
KBio3_002965
DTXSID10859420
LUKBXSAWLPMMSZ-UHFFFAOYSA-N
Bio2_000397
Bio2_000877
HMS3267J06
HMS3394I09
HMS3426I09
HMS3654D04
HMS3871F03
AKOS025244084
SB17273
SMP1_000257
NCGC00017352-23
NCI60_002840
SY014849
DB-030329
DB-072954
DB-139429
NS00010180
NS00096464
5-[2-(4-Hydroxyphenyl)ethenyl]-1,3-benzenediol
Q60998680