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Piceatannol

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Identification
Molecular formula
C14H12N2O2
CAS number
10083-24-6
IUPAC name
4-[2-(4-carbamimidoylphenyl)vinyl]benzamidine
State
State

At room temperature, Piceatannol exists in a solid state. It is stable under normal conditions and is typically found as a crystalline powder.

Melting point (Celsius)
223.00
Melting point (Kelvin)
496.15
Boiling point (Celsius)
662.40
Boiling point (Kelvin)
935.60
General information
Molecular weight
243.26g/mol
Molar mass
243.2560g/mol
Density
1.3200g/cm3
Appearence

Piceatannol is typically an off-white to beige solid that crystallizes. It is noted for its polyphenolic structure, consisting of hydroxyl groups attached to its aromatic rings, which can contribute to its characteristic appearance.

Comment on solubility

Solubility of 4-[2-(4-carbamimidoylphenyl)vinyl]benzamidine

The solubility of 4-[2-(4-carbamimidoylphenyl)vinyl]benzamidine can be characterized as follows:

  • Polar Solvents: This compound is likely to exhibit solubility in polar solvents such as water and alcohols due to the presence of nitrogen groups that engage in hydrogen bonding.
  • Non-Polar Solvents: Solubility in non-polar solvents (like hexane or benzene) may be limited due to the strong polar character of the amino groups.
  • pH Dependency: The solubility may also depend on the pH of the solution, as the protonation states of the amine functional groups can affect its overall solubility.
  • Temperature Effect: Generally, increasing the temperature may enhance the solubility of compounds, facilitating greater interaction with the solvent molecules.

Overall, this compound's solubility can be affected by various factors, and experimental validation is essential. As with many organic compounds, the interplay between polarity, temperature, and solvent choice plays a critical role in determining its solubility profile.

Interesting facts

Interesting Facts about 4-[2-(4-carbamimidoylphenyl)vinyl]benzamidine

4-[2-(4-carbamimidoylphenyl)vinyl]benzamidine is a fascinating compound that has drawn the attention of researchers in various fields due to its unique structure and potential applications. Here are some key points to consider:

  • Structural Complexity: This compound features a vinylic linkage that connects two aromatic rings, resulting in an intriguing molecular architecture. The presence of the –C(=NH)NH group adds to its significance, as it plays a crucial role in the compound's biological activity.
  • Potential Biological Activity: Compounds like this often exhibit pharmacological properties, making them candidates for various drug development projects. The carbamimidoyl moiety is of particular interest in medicinal chemistry due to its capability to mimic certain biomolecules.
  • Role in Research: This compound is sometimes explored in the context of enzymatic inhibition, particularly in the realm of protease research. Its ability to interact with active sites of enzymes could lead to new therapeutic strategies.
  • Synthetic Methods: The synthesis of 4-[2-(4-carbamimidoylphenyl)vinyl]benzamidine can involve multiple steps, typically including reactions such as condensation and coupling. Understanding these routes provides insights into organic synthesis techniques and the manipulation of functional groups.
  • Research Implications: There's a growing interest in the exploration of similar compounds for developing novel anticancer agents. By understanding how this compound functions, scientists can design more effective treatments.

In conclusion, 4-[2-(4-carbamimidoylphenyl)vinyl]benzamidine is more than just a compound; it represents the intersection of organic chemistry and pharmacology. As research continues, we may discover even more about its potential applications and significance in the field.

Synonyms
DTXSID30861808
4,4'-ethene-1,2-diyldibenzenecarboximidamide
4,4'-(Ethene-1,2-diyl)di(benzene-1-carboximidamide)
Ba 2652;Stilbamidin
NSC35605
NCIStruc1_000990
NCIStruc2_001283
SCHEMBL889782
DTXCID80810684
AAA12206
NCI60_003209
4,4'-Stilbenedicarboxamidine, diisethionate
NS00041372