Fenobucarb
- Molecular formula
- C12H17NO3
- CAS Number
- 3766-81-2
- IUPAC Name
- [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate
- Molecular Weight
- 221.27g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1000g/cm3
- Synonyms
- NSC-222513
Identification
Exploring [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate
[3-(but-2-enoylamino)phenyl] N-isopropylcarbamate is a fascinating compound known for its unique chemical structure and potential applications in the fields of pharmaceuticals and biochemistry. As a derivative of carbamic acid, it participates in various biological processes, making it quite significant in research.
Key Features
- Amide Bond: The compound contains an amide functional group that is crucial in the formation of peptide bonds, highlighting its importance in protein structure.
- Unsaturated Moiety: The presence of a but-2-enoyl group introduces unsaturation, which can influence reactivity and interaction with biological systems.
- Substituted Aromatic Ring: The phenyl group in the structure contributes to the hydrophobic character and electronic properties that can modulate biological activity.
This compound is not only an interesting molecular entity but also acts as a probe for studying various chemical reactions and mechanisms. The combination of its functional groups allows scientists to explore potential therapeutic activities, such as:
- Antimicrobial properties
- Anticancer activity
- Enzyme inhibitors
With ongoing research, [3-(but-2-enoylamino)phenyl] N-isopropylcarbamate exemplifies the marriage of organic chemistry and medicinal applications, showcasing how intricate molecular design can pave the way for innovative solutions in health and science. As one chemist aptly said, "The beauty of chemistry lies in the endless possibilities of how simple molecules can lead to complex biological interactions."