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Aurantioclavine

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Identification
Molecular formula
C15H9N3O3
CAS number
91414-64-5
IUPAC name
2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile
State
State

At room temperature, aurantioclavine exists in a solid state. It is typically handled as a powder or crystalline solid during chemical analysis or when utilized in reactions.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.00
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.00
General information
Molecular weight
315.30g/mol
Molar mass
315.2960g/mol
Density
1.4210g/cm3
Appearence

Aurantioclavine is a crystalline compound characterized by an orange to yellow-brown hue. It is often found in its crystal form and exhibits a vivid color that makes it easily distinguishable in laboratory settings.

Comment on solubility

Solubility of 2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile

The solubility of 2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile (C15H9N3O3) can be influenced by a variety of factors due to its complex molecular structure and functional groups. Understanding its solubility characteristics is essential for various applications. Here are some key points to consider:

  • Water Solubility: The presence of multiple hydroxy groups (–OH) suggests that this compound may exhibit some degree of solubility in water. These polar groups can form hydrogen bonds with water molecules, enhancing solubility.
  • Solvent Polarity: In polar solvents, the solubility is likely to increase due to dipole-dipole interactions, whereas in non-polar solvents, solubility is expected to be low. Therefore, solvent choice is critical.
  • Temperature Effect: Solubility can also be affected by temperature; typically, higher temperatures can enhance the solubility of many compounds.
  • pH Dependency: Changes in pH can impact the ionization of amino and hydroxyl groups, further influencing solubility.

In summary, while the exact solubility data for 2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile may require further empirical study, its multiple functional groups point towards potentially interesting solubility behavior in various environments. Careful consideration of these factors is essential for practical applications and synthesis processes.

Interesting facts

Interesting Facts about 2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile

2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile, commonly referred to as a derivative of flavonoid compounds, is an intriguing molecule with various noteworthy aspects:

  • Structure: This compound exemplifies how amino groups can enhance the reactivity of diene systems, signifying a fascinating aspect of organic chemistry where functional groups play crucial roles in chemical behavior.
  • Biological Activity: Compounds with a similar structure have been investigated for potential therapeutic effects, particularly their ability to act as antioxidants, which can help combat oxidative stress in biological systems.
  • Natural Products: The presence of the hydroxyphenyl group suggests that this compound may share similarities with natural flavonoids, which are known for their diverse biological functions including anti-inflammatory and anti-cancer properties.
  • Synthesis: The synthesis of such compounds often involves multi-step organic reactions, showcasing the creative methodologies chemists use to construct complex molecules from simpler ones.
  • Research Interest: Researchers are often intrigued by the photochemical properties of diene systems, which can lead to valuable applications in material science and photonics.

In the words of famous chemist "The essence of chemical research lies in the interplay of structure and reactivity." Studying compounds like 2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile allows chemists to explore this interplay further, contributing to our understanding of both synthetic methodologies and their potential applications.

Synonyms
(Z)-Tyrphostin A51
(Z)-AG-183
2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile
Q27166454