Carbofuran
- Molecular formula
- C12H15Cl2NO2
- CAS Number
- 1563-66-2
- IUPAC Name
- 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate
- Molecular Weight
- 221.11g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2130g/cm3
- Synonyms
- NSC379373
Identification
Interesting Facts about 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate
2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate, commonly known as a potent inhibitor, is a compound that reveals fascinating insights into chemical functionality and applications in various fields.
Key Features
- Biological Activity: This compound exhibits significant biological activity, making it valuable in pharmaceutical research. Its mechanism often involves interactions with neurotransmitter systems, influencing a variety of biological responses.
- Pest Control: Due to its carbamate structure, it can function as an insecticide, illustrating its applicability in agriculture. Carbamates are known for their effectiveness against a wide range of pests.
- Synthetic Pathways: The synthesis of this compound involves multi-step organic reactions which could include nucleophilic substitutions and coupling reactions, making it a prime candidate for educational purposes in organic chemistry courses.
- Structure-Activity Relationship (SAR): The modification of the diethylamino and dichlorophenyl portions can lead to variations in biological activity, shedding light on the importance of SAR in drug design.
Anecdotal Insights
As a chemistry student, exploring compounds like this can ignite a passion for research. Consider this interesting quote from a seasoned chemist: "Understanding the intricacies of molecular interactions opens doors to innovation." This highlights why studying such compounds is not merely academic but can lead to real-world solutions.
Ultimately, 2-(diethylamino)ethyl N-(3,5-dichlorophenyl)carbamate embodies the intersection of chemistry, biology, and practical applications, encouraging future scientists to unlock the potential hidden within its structure.