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CNS-5161

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Identification
Molecular formula
C17H15NO2
CAS number
31306-45-1
IUPAC name
3-(3,4-dimethoxyphenyl)-2-phenyl-prop-2-enenitrile
State
State

At room temperature, the compound is typically in a solid state. It is often handled as a crystalline powder.

Melting point (Celsius)
177.90
Melting point (Kelvin)
451.05
Boiling point (Celsius)
488.90
Boiling point (Kelvin)
762.05
General information
Molecular weight
265.31g/mol
Molar mass
265.3110g/mol
Density
1.0937g/cm3
Appearence

The compound, 3-(3,4-dimethoxyphenyl)-2-phenyl-prop-2-enenitrile, appears as a crystalline solid.

Comment on solubility

Solubility of 3-(3,4-dimethoxyphenyl)-2-phenyl-prop-2-enenitrile

The solubility of 3-(3,4-dimethoxyphenyl)-2-phenyl-prop-2-enenitrile can often be influenced by various factors, including the molecular structure and the presence of functional groups. This compound is characterized by its aromatic systems and nitrile group, which can affect its interactions with solvents.

Key solubility considerations include:

  • Aromatic Character: The presence of multiple aromatic rings generally increases the degree of hydrophobic interactions, leading to lower solubility in polar solvents such as water.
  • Nitrile Group: The -C≡N group is polar and can interact with polar solvents, potentially increasing solubility in certain conditions.
  • Dimethoxy Substituents: The methoxy groups can introduce some polarity, enabling solubility in a range of organic solvents, primarily those that are non-polar to slightly polar.

As a result, this compound is likely to exhibit:

  • Higher solubility in organic solvents such as ethanol, acetone, or dichloromethane.
  • Limited solubility in water and highly polar solvents due to its largely hydrophobic structure.

Understanding the solubility profile of this compound is crucial for its applications, be it in synthesis, formulation, or biological activity. Always consult relevant solubility data and perform practical tests to confirm solubility under specific conditions.

Interesting facts

Interesting Facts about 3-(3,4-dimethoxyphenyl)-2-phenyl-prop-2-enenitrile

This compound is a striking example of synthetic versatility in organic chemistry, often attracting interest due to its intriguing structural characteristics. Here are some essential points that encapsulate the significance and potential of this molecule:

  • Structural Diversity: The presence of both a nitrile functional group and multiple aromatic rings makes this compound a fascinating subject for studying the effects of structure on reactivity.
  • Biological Activity: Compounds featuring an aromatic nitrile moiety are often investigated for their potential biological activities, including anti-inflammatory and anticancer properties.
  • Applications in Material Science: The unique electronic properties arising from its conjugated system may lead to applications in organic electronics, such as organic photovoltaics and light-emitting diodes.
  • Synthesis Challenges: The synthesis of such compounds can be a complex endeavor, often requiring intricate reaction conditions and strategies to ensure high yield and purity.

This compound exemplifies the multifaceted nature of organic chemistry, where simple modifications to a molecular framework can lead to significant changes in properties and applications. It highlights the ongoing exploration in synthetic methodologies that push the boundaries of our understanding and ability in assembling complex organic molecules.

In the words of renowned chemist August Kekulé, "Chemistry is a science of transformations," and compounds like 3-(3,4-dimethoxyphenyl)-2-phenyl-prop-2-enenitrile embody this transformative spirit brilliantly.


Synonyms
Oprea1_236957
SCHEMBL8361937
3-(3,4-dimethoxyphenyl)-2-phenyl-prop-2-enenitrile