Interesting facts
Interesting Facts about 2-[methyl(prop-2-ynyl)amino]phenyl N-methylcarbamate
2-[methyl(prop-2-ynyl)amino]phenyl N-methylcarbamate is a compound that showcases the fascinating intersection of organic chemistry and applications in various fields, including agriculture and pharmaceuticals. Here are some engaging points about this intriguing compound:
- Biodiversity in Chemistry: This compound is a derivative of carbamate, a class of organic compounds known for their utility in pesticides and pharmaceuticals. Carbamates play a critical role in the development of insecticides that are designed to be less harmful to non-target species, illustrating the ongoing efforts to create safer agricultural practices.
- Mechanism of Action: Carbamates, including this compound, generally work as acetylcholinesterase inhibitors. By inhibiting this enzyme, they disrupt the breakdown of acetylcholine, leading to an accumulation of this neurotransmitter, which can eventually cause paralysis in pests. This mechanism draws interest for those studying neurobiology and pharmacology.
- Structural Versatility: The structure of 2-[methyl(prop-2-ynyl)amino]phenyl N-methylcarbamate illustrates how modifications to functional groups can lead to significant changes in biological activity. This versatility demonstrates the importance of structure-activity relationships (SAR) in drug design.
- Historical Context: The development of carbamate pesticides traces back to the mid-20th century when they were introduced as alternatives to organophosphates. As scientific understanding of environmental safety evolved, the focus on creating compounds like this one that balance efficacy with safety became paramount.
- Research Potential: Ongoing research into carbamate derivatives, including this specific compound, may lead to new findings in the fields of medicinal chemistry, where scientists are continuously exploring the potential for these compounds to be employed as therapeutic agents.
In the grand narrative of chemical science, 2-[methyl(prop-2-ynyl)amino]phenyl N-methylcarbamate stands as a testament to the creativity and ingenuity of chemists. With its unique structure and diverse applications, it exemplifies the dualities of innovation and safety in modern chemistry.
Synonyms
CGA 13608
23504-07-6
BRN 2979833
C-17018
AI3-27701
C 17018
Phenol, 2-(methyl-2-propynylamino)-, methylcarbamate
2-(Methyl-2-Propynylamino)phenyl N-methylcarbamate
Carbamic Acid, [2-(methyl-2-propynylamino)phenyl]-, methyl ester
Carbamic Acid, (2-(methyl-2-propynylamino)phenyl)-, methyl ester
RefChem:331487
GJYRCEALCUOYBO-UHFFFAOYSA-N
Carbamic acid, methyl-, o-(methyl-2-propynylamino)phenyl ester
Phenol, 2-(methyl-2-propynylamino)-, methylcarbamate (ester)
CARBAMIC ACID, METHYL-, 2-(N-METHYL-N-(2-PROPYNYL)AMINO)PHENYL ESTER
SCHEMBL435129
DTXSID00946191
N-Methylcarbamic acid o-[methyl(2-propynyl)amino]phenyl ester
2-[Methyl(2-propynyl)amino]phenyl methylcarbamate #
2-[Methyl(prop-2-yn-1-yl)amino]phenyl hydrogen methylcarbonimidate
Phenol, 2-(methyl-2-propyn-1-ylamino)-, methylcarbamate (ester)
Solubility of [2-[methyl(prop-2-ynyl)amino]phenyl] N-methylcarbamate
The solubility of [2-[methyl(prop-2-ynyl)amino]phenyl] N-methylcarbamate can be influenced by several factors, such as temperature, pH, and the presence of other solutes. Here are some key points to consider:
Overall, the solubility of this compound is characterized by its unique structural features that lead to variable behavior in different environments. The statement that "solubility is key to bioavailability and reactivity" holds especially true for [2-[methyl(prop-2-ynyl)amino]phenyl] N-methylcarbamate, as it determines its effectiveness in various applications.