Synthetic Route of 2213-63-0, New Advances in Chemical Research in 2021. Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2. In a article，once mentioned of 2213-63-0
The synthesis of the quinoxaline-bridged resorcin[4]arene cavitand 1 was accomplished from 2-[3,5-di(tertbutyl)phenyl]acetaldehyde via formation of the intermediate octol 2. Such cavitands are known to occur in an open ‘kite’ conformation at low temperature (<213 K) but to adopt a 'vase' conformation at elevated temperatures (> 318 K). We discovered that protonation of cavitand 1 at room temperature by common acids, such as CF3COOH, also causes reversible switching from ‘vase’ to ‘kite’, and that this conformational change can be conveniently monitored by both 1H-NMR and UV/VIS spectroscopy.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 2213-63-0, and how the biochemistry of the body works.Synthetic Route of 2213-63-0
Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1547 | ChemSpider