Carbaryl
- Molecular formula
- C12H11NO2
- CAS Number
- 63-25-2
- IUPAC Name
- (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate
- Molecular Weight
- 201.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2510g/cm3
- Synonyms
- alpha-Fenchyl alcohol methylcarbamate
Identification
Interesting Facts About (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate
(1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate is a fascinating compound that falls within the class of carbamates, which are known for their versatility and wide-ranging applications. This particular structure is characterized by its complex bicyclic carbon framework, depicting a unique blend of rigidity and reactivity.
Key Features of the Compound:
- Carbamate Functionality: As a member of the carbamate family, this compound showcases the ability to act as a nutrient and environmental stress mitigator in agricultural applications.
- Synthetic Applications: It serves as an important intermediate in the synthesis of various pharmaceuticals, illustrating its significance in medicinal chemistry.
- Biological Activity: Due to its structural features, it has been studied for potential biological activities, making it a point of interest in drug design and discovery.
This compound's intriguing structure leads to diverse reactivity patterns, marking its importance in research. As chemists explore new uses or modifications of this compound, they often remark on its implications in enhancing the efficiency of chemical reactions. As one prominent chemist once said, "The chemistry of carbamates offers not just complexity, but an opportunity to innovate."
Research on (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate continues to evolve, revealing potential contributions to sustainable practices in agriculture and environmentally friendly pest control methods. Its unique structural attributes open the door to numerous possibilities in both academic and industrial chemistry, making it an area ripe for exploration.