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3-(3-methoxyphenyl)prop-2-enenitrile

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Identification
Molecular formula
C10H9NO
CAS number
5398-23-8
IUPAC name
3-(3-methoxyphenyl)prop-2-enenitrile
State
State

At room temperature, it exists in a solid state, often obtained as crystalline powder.

Melting point (Celsius)
56.00
Melting point (Kelvin)
329.15
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
159.19g/mol
Molar mass
159.1880g/mol
Density
1.0896g/cm3
Appearence

3-(3-Methoxyphenyl)prop-2-enenitrile is typically a colorless to pale yellow crystalline solid. It is often used in organic synthesis due to its distinctive structure that combines aromatic and nitrile functional groups.

Comment on solubility

Solubility of 3-(3-methoxyphenyl)prop-2-enenitrile

The solubility of 3-(3-methoxyphenyl)prop-2-enenitrile, known for its unique structural properties, is influenced by several factors:

  • Polarity: Due to the presence of the methoxy group, the compound exhibits a degree of polarity which can enhance its solubility in polar solvents.
  • Hydrophobic interactions: The phenyl rings add hydrophobic character, which can limit solubility in strictly aqueous environments.
  • Solvent choice: This compound is likely more soluble in organic solvents such as ethanol, acetone, or dimethyl sulfoxide (DMSO) than in water.
  • Temperature: Solubility can also increase with temperature, often necessary for dissolving organic compounds.

In summary, while 3-(3-methoxyphenyl)prop-2-enenitrile is moderately soluble in polar organic solvents, its solubility in water is limited. The interplay between its hydrophobic and hydrophilic portions dictates its behavior in various solvent systems. Understanding these factors allows for better handling and application in chemical processes.

Interesting facts

Interesting Facts about 3-(3-methoxyphenyl)prop-2-enenitrile

3-(3-methoxyphenyl)prop-2-enenitrile is a fascinating compound that belongs to the class of organic compounds known as nitriles. These compounds are characterized by the presence of a cyano group (−C≡N), which imparts unique properties and reactivity. Here are some key points to consider:

  • Biological Relevance: Nitriles are known for their diverse roles in biological systems. Some nitriles exhibit significant biological activity, making compounds like 3-(3-methoxyphenyl)prop-2-enenitrile of interest in pharmaceutical research.
  • Versatile Synthesis: This compound can be synthesized through versatile organic reactions, allowing for modifications that can lead to derivatives with new and improved properties.
  • Potential Applications: The presence of the methoxy group in the structure suggests potential applications in the field of agrochemicals or as precursors for new materials in organic electronics.
  • Research Importance: Compounds with a similar structure have been studied for their potential antioxidant and anticancer properties, which means that understanding their mechanism of action could lead to significant advancements in medicine.

As a student or researcher, appreciating the intricate structure and functionality of 3-(3-methoxyphenyl)prop-2-enenitrile is crucial in exploring its implications in various fields such as medicinal chemistry, agrochemistry, and materials science. This compound serves as a reminder of the intricate relationships between structure and function in chemistry, highlighting the endless possibilities for discovery and innovation.

Synonyms
DTXSID101291936
3-(3-Methoxyphenyl)-2-propenenitrile
28446-69-7
RefChem:492104
DTXCID301722519
112-008-2
3-METHOXYCINNAMONITRILE
SCHEMBL8928082
CDGKYGSIBOJVCY-UHFFFAOYSA-N
AKOS017436827