Interesting facts
Interesting Facts about (2-chloro-5-sec-butyl-phenyl) N-methylcarbamate
(2-chloro-5-sec-butyl-phenyl) N-methylcarbamate is a fascinating compound that finds its significance in the field of chemical research and applications. Here are some noteworthy points about this intriguing substance:
- Class Structure: This compound belongs to the class of carbamates, which are esters or salts of carbamic acid. Carbamates are widely recognized for their applications in agriculture as pesticides and herbicides, as well as in the pharmaceutical industry.
- Chlorination Impact: The presence of the 2-chloro group can greatly influence the reactivity and biological activity of the compound. Chlorinated compounds are known for their enhanced stability and lipophilicity, which can affect their biological interactions.
- Sec-butyl Influence: The 5-sec-butyl group contributes to the compound's unique steric and electronic properties. This branched alkyl group can affect the compound's solubility and reactivity, making it interesting for various chemical applications.
- Synthetic Utility: The synthesis of N-methylcarbamate derivatives like this one is significant in the field of organic chemistry. They serve as building blocks for more complex organic molecules, thus playing a crucial role in the development of new materials.
- Biological Relevance: Studies on similar carbamates have shown that they may exhibit herbicidal and insecticidal properties, making them valuable in agricultural chemistry. Research continues to explore their potential in pest control while maintaining safety for non-target organisms.
In summary, (2-chloro-5-sec-butyl-phenyl) N-methylcarbamate exemplifies the intricate interplay of structure and function in organic chemistry. Its unique features open up pathways for continued research and development in scientific fields.
Synonyms
2917-19-3
2-Chloro-5-(1-methylpropyl)phenol methylcarbamate
Chevron RE 5655
Cal Chem 5655
Ortho-5655
RE 5655
ENT 27,128
AI3-27128
2-Chloro-5-(1-methylpropyl)phenyl methylcarbamate
3-(1-Methylpropyl)-6-chlorophenyl methylcarbamate
Phenol, 2-chloro-5-(1-methylpropyl)-, methylcarbamate
Carbamic acid, methyl-, 3-sec-butyl-6-chlorophenyl ester
CARBAMIC ACID, METHYL-, 5-sec-BUTYL-2-CHLOROPHENYL ESTER
Carbamic acid, methyl-, 2-chloro-5-(1-methylpropyl)phenyl ester
DTXSID60951766
2-Chloro-5-(1-methylpropyl)phenol 1-(N-methylcarbamate)
5-(Butan-2-yl)-2-chlorophenyl hydrogen methylcarbonimidate
Solubility of (2-chloro-5-sec-butyl-phenyl) N-methylcarbamate
The solubility of (2-chloro-5-sec-butyl-phenyl) N-methylcarbamate is an interesting topic for discussion, particularly concerning its applications in various chemical processes. This compound, which contains both a carbamate functional group and a chloro substitution, showcases unique solubility characteristics influenced by its molecular structure.
Factors Affecting Solubility
Several factors contribute to the solubility behavior of this compound:
Practical Implications
In practice, the solubility of (2-chloro-5-sec-butyl-phenyl) N-methylcarbamate can vary widely based on the solvent used. It is likely to possess:
Understanding these solubility dynamics is crucial for its applications in fields such as organic synthesis and biochemical research. Overall, the solubility of this compound exemplifies the delicate balance between molecular structure and solvent interactions, revealing the fascinating complexity of chemical solubility.