Fenobucarb
- Molecular formula
- C12H17NO3
- CAS Number
- 3766-81-2
- IUPAC Name
- [3-(butanoylamino)phenyl] N-methylcarbamate
- Molecular Weight
- 207.24g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1470g/cm3
- Synonyms
- 17814-27-6
Identification
Interesting Facts about [3-(butanoylamino)phenyl] N-methylcarbamate
[3-(butanoylamino)phenyl] N-methylcarbamate is an intriguing compound that blends organic chemistry with medicinal applications. Here are some fascinating insights into its structure and uses:
- Unique Structure: This compound features a phenyl ring substituted with a butanoylamino group, highlighting the versatility of amine functionalities in organic synthesis.
- Carbamate Moiety: The presence of a carbamate functional group is significant, as it is frequently encountered in pharmaceuticals and agrochemicals, providing a linkage that enhances compound stability.
- Biological Activity: Compounds like this one can exhibit diverse biological properties, making them potential candidates in drug discovery, particularly in the development of agrochemicals and therapeutic agents.
- Synthesis Routes: The synthetic pathways to obtain this compound often involve nucleophilic substitutions or acylation reactions which are foundational concepts in organic chemistry.
- Research Relevance: The exploration of compounds with similar structures contributes to the understanding of structure-activity relationships (SAR), crucial for tailoring compounds with desired bioactivity.
In summary, [3-(butanoylamino)phenyl] N-methylcarbamate is not just a compound of theoretical interest; it embodies a crucial intersection of chemistry and biology, representing how small changes in chemical structure can lead to significant variations in functionality. As highlighted by renowned chemist Robert H. Grubbs, "Chemistry is the study of matter, but I prefer to view it as the study of change." This compound exemplifies that change in action.