4-Methoxycinnamonitrile

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Identification

Molecular formula
C10H9NO
CAS Number
1676-64-0
IUPAC Name
3-(4-methoxyphenyl)prop-2-enenitrile
Molecular Weight
159.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0370g/cm3
Synonyms
3-(4-methoxyphenyl)prop-2-enenitrile
Interesting facts

Exploring 3-(4-methoxyphenyl)prop-2-enenitrile

3-(4-methoxyphenyl)prop-2-enenitrile is a fascinating compound that bridges the realms of organic chemistry and materials science. Here are some intriguing aspects of this compound:

  • Structural Features: The compound features a prop-2-enenitrile backbone, which includes a nitrile (-C≡N) functional group. This configuration makes it a relevant subject for studies in reactivity and synthesis within organic chemistry.
  • Substituent Influence: The presence of the 4-methoxyphenyl group greatly influences its chemical properties. This methoxy (-OCH3) substituent can enhance electron donation, impacting the compound’s reactivity and interaction with other species.
  • Reactivity: Compounds like 3-(4-methoxyphenyl)prop-2-enenitrile are known to undergo various chemical reactions, including nucleophilic additions and electrophilic substitutions. Understanding these reactions can provide insight into synthetic pathways in organic synthesis.
  • Potential Applications: The compound may find utility in material science, organic electronics, or as a precursor in dye synthesis due to its unique structural attributes, including its conjugated system, which is beneficial for light absorption.
  • Research Significance: The study of compounds with similar structures can lead to advancements in the development of pharmaceuticals, agrochemicals, and functional materials. Their diverse applications make them significant in both industrial and academic research.

In the context of research and practical application, the exploration of 3-(4-methoxyphenyl)prop-2-enenitrile offers a glimpse into the intricate world of organic compounds and their versatility in modern chemistry.

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