Interesting facts
Interesting Facts About 1-Phenylprop-2-ynyl Carbamate
1-Phenylprop-2-ynyl carbamate is a fascinating compound that showcases the intersection of organic chemistry and medicinal applications. Here are several key points that highlight its significance:
- Structure and Function: This compound belongs to the class of carbamates, which are esters of carbamic acid. Its unique structure, featuring a phenyl group and an alkyne, contributes to its interesting chemical reactivity and potential pharmaceutical properties.
- Applications in Medicine: Compounds like 1-phenylprop-2-ynyl carbamate are studied for their biological activities. Researchers investigate their potential as anti-cancer agents due to their ability to disrupt cellular pathways in tumor cells.
- Synthetic Versatility: The synthesis of 1-phenylprop-2-ynyl carbamate can provide insights into reaction mechanisms. It serves as a platform for generating a wide variety of derivatives that may exhibit enhanced biological activity.
- Study of Reaction Mechanisms: As a subject in organic chemistry, this compound offers a great opportunity to explore reaction mechanisms, particularly in the context of nucleophilic substitution reactions that involve carbamates.
- Environmental Considerations: The study of carbamate derivatives, such as this one, extends to their environmental impact. Understanding their degradation pathways is important for assessing their safety and persistence in ecological systems.
In the words of renowned chemist Linus Pauling, “The greatest benefit we can give to the world is to discover new knowledge.” This serves as a reminder of the potential embedded within compounds like 1-phenylprop-2-ynyl carbamate as we continue to explore their properties and applications.
Overall, 1-phenylprop-2-ynyl carbamate embodies the rich complexity of chemical compounds and the endless possibilities they hold for scientific discovery.
Synonyms
Carfimate
3567-38-2
Carfimat
1-Phenyl-2-propynyl carbamate
Phenylethynylcarbinol carbamate
Carfimate [INN]
Carfimato
Carfimatum
Nirvotin
1-phenylprop-2-yn-1-yl carbamate
Carfimatum [INN-Latin]
Carfimato [INN-Spanish]
alpha-Ethynylbenzyl carbamate
X9N1XKR2OS
alpha-Ethynylbenzenemethanol carbamate
BRN 3200625
Carbamic acid, 1-phenyl-2-propynyl ester
Carbammato di feniletinilcarbinolo
Carbammato di feniletinilcarbinolo [Italian]
CARFIMATE [MI]
Benzenemethanol, alpha-ethynyl-, carbamate
DTXSID70863200
BENZYL ALCOHOL, alpha-ETHYNYL-, CARBAMATE
4-06-00-04067 (Beilstein Handbook Reference)
Carfimatum (INN-Latin)
Carfimato (INN-Spanish)
DTXCID80811858
Benzenemethanol, alpha-ethynyl-, carbamate (9CI)
985-353-7
1-phenylprop-2-ynyl carbamate
UNII-X9N1XKR2OS
1-phenyl-2-propinylcarbamat
SCHEMBL1648782
CHEMBL2105609
1-phenylprop-2-yn-1-ylcarbamate
CHEBI:134809
DAA56738
AKOS006272297
HY-W171071
DA-56807
CS-0232220
NS00123582
EN300-1266214
Q27293733
Z1198155485
Solubility of 1-Phenylprop-2-ynyl Carbamate
1-Phenylprop-2-ynyl carbamate, with its complex structure, showcases intriguing solubility properties that make it noteworthy in various applications. When discussing solubility, it's essential to consider the following aspects:
In conclusion, while 1-phenylprop-2-ynyl carbamate may exhibit limited solubility in aqueous environments, it displays a better affinity for organic solvents, thus expanding its potential uses in chemical synthesis and applications. As emphasized by solubility principles, "like dissolves like," making the choice of solvent critical when working with this compound.