N-[(4-dimethylamino)phenyl]acrylamide
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- Molecular formula
- C12H14N2O
- CAS Number
- 16400-06-5
- IUPAC Name
- 2-cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide
- Molecular Weight
- 201.25g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1940g/cm3
- Synonyms
- ALPHA-CYANO-4-(DIMETHYLAMINO)-CINNAMAMIDE
Identification
Interesting facts
Exploring 2-Cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide
2-Cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide is a fascinating chemical compound that plays a significant role in various fields, particularly in organic chemistry and pharmaceuticals. Here are some intriguing facts about this compound:
- Structure: This compound features a unique molecular framework that includes a cyano group, an amide, and a dimethylamino group. This diverse structure allows it to participate in a wide range of chemical reactions.
- Reactivity: The presence of the cyano and amide functional groups makes this compound quite reactive. It can undergo nucleophilic additions, facilitating the formation of more complex molecules.
- Biological Activity: Many compounds with similar structures have been investigated for their pharmaceutical properties, potentially serving as intermediates in drug synthesis. The dimethylamino group is known to enhance solubility and biological activity.
- Applications: Its derivatives are often explored for use in medicinal chemistry. They are connected to therapeutic agents that target various diseases, including cancer.
- Synthetic Pathways: The synthesis of 2-cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide can involve multiple methods, including the condensation of reactive precursors. This positions it as a significant compound in synthetic routes.
- Research Potential: Due to its intriguing properties, this compound is a subject of scientific research, including studies aimed at developing new antitumor or antiviral agents.
As students and researchers delve into the realm of organic compounds, 2-cyano-3-[4-(dimethylamino)phenyl]prop-2-enamide serves as an excellent example of how structural nuances translate into significant chemical behaviors and applications. Its ability to participate in a myriad of reactions while also holding potential therapeutic benefits underscores the beauty and complexity of organic chemistry.