Interesting facts
Interesting Facts about S-(2-chloroallyl) N,N-diethylcarbamothioate
S-(2-chloroallyl) N,N-diethylcarbamothioate, often referred to as a carbamate derivative, is a compound of significant interest in various fields, particularly in agriculture and chemistry. Here are some intriguing insights into this compound:
- Agricultural Applications: This compound has been utilized as a pesticide, providing effective control over a range of pests. Its unique structure enhances its ability to target specific organisms while minimizing effects on non-target species.
- Mechanism of Action: Understanding how S-(2-chloroallyl) N,N-diethylcarbamothioate works at the molecular level is crucial. It acts by interfering with the insect's nervous system, demonstrating how structural components can play a vital role in biological activity.
- Environmental Safety: One of the critical factors for any pesticide today is its environmental impact. Ongoing research into the environmental persistence and toxicity profiles of carbamate compounds, including this one, aims to ensure safer agricultural practices.
- Historical Context: The discovery and development of carbamates trace back several decades, marking significant milestones in chemical research. Many scientists have contributed to understanding the synthesis and application of these compounds, which highlights the collaborative nature of scientific exploration.
- Research Opportunities: There are still numerous avenues for research surrounding S-(2-chloroallyl) N,N-diethylcarbamothioate, especially in modifying its molecular structure to enhance efficacy and reduce toxicity. Such studies can lead to innovative agricultural solutions.
In summary, S-(2-chloroallyl) N,N-diethylcarbamothioate encapsulates the dynamic intersection of chemistry and agriculture, showcasing the importance of chemical compounds in addressing real-world challenges. Scientists continuously strive to balance efficacy with safety, making this compound a fascinating subject for further investigation.
Synonyms
Diethylthiocarbamic acid S-2-chloroallyl ester
18283-60-8
BRN 1772270
CARBAMIC ACID, DIETHYLTHIO-, S-2-CHLOROALLYL ESTER
2-Chloroallyl N,N-diethyl thiolcarbamate
4-04-00-00387 (Beilstein Handbook Reference)
SCHEMBL6304971
DTXSID00171345
Solubility of S-(2-chloroallyl) N,N-diethylcarbamothioate
The solubility of S-(2-chloroallyl) N,N-diethylcarbamothioate is an intriguing aspect that influences its applications in various fields. This compound presents a unique solubility profile due to its specific chemical structure and functional groups.
Generally, the solubility characteristics of this compound can be summarized as follows:
Moreover, it is often said that "like dissolves like," which is essential when considering the solubility of chemical compounds. In the case of S-(2-chloroallyl) N,N-diethylcarbamothioate, the interaction with solvents will depend greatly on its molecular structure and the polarity of the solvent used.
In summary, the solubility of S-(2-chloroallyl) N,N-diethylcarbamothioate is a critical factor for its practical applications, highlighting the necessity to carefully select appropriate solvents in any experimental or industrial setting.