Cinnamamide
- Molecular formula
- C10H11NO2
- CAS Number
- 4041-59-6
- IUPAC Name
- N-(2-hydroxyethyl)-3-phenyl-prop-2-enamide
- Molecular Weight
- 177.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1768g/cm3
- Synonyms
- N-(2-Hydroxyethyl)-3-phenylpropenamide
Identification
Interesting Facts About N-(2-hydroxyethyl)-3-phenyl-prop-2-enamide
N-(2-hydroxyethyl)-3-phenyl-prop-2-enamide, often referred to in scientific literature for its versatile applications, showcases the fascinating intersection of organic chemistry and materials science. Here are some noteworthy aspects of this compound:
- Functional Versatility: This compound contains both an amide and an allylic double bond, granting it unique reactivity and making it valuable in many chemical synthesis processes.
- Biological Activity: Compounds of this nature can exhibit significant biological properties, including antimicrobial and anti-inflammatory effects, making them of particular interest in pharmaceutical development.
- Building Block in Synthesis: Due to its structure, N-(2-hydroxyethyl)-3-phenyl-prop-2-enamide is often employed as a building block in the synthesis of larger, more complex molecules, particularly in the development of polymers and functional materials.
- Research Interest: Scientists are increasingly focusing on derivatives of this compound to enhance their properties, potentially leading to innovative applications in drug design and materials engineering.
As noted by chemists in the field, "the unique structural features of such compounds frequently lead to unexpected properties and functionalities." This highlights the importance of N-(2-hydroxyethyl)-3-phenyl-prop-2-enamide not just as a standalone substance, but as a pivotal entity in ongoing research and development.
In summary, N-(2-hydroxyethyl)-3-phenyl-prop-2-enamide is a compound rich with potential, bridging organic chemistry with practical applications that could shape future technologies and therapies.