Chemical Properties and Facts of 7467-91-6

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The delocalization of electron density upon tautomerization of a proton across a conjugated bridge can alter the strength of hydrogen bonds. This effect has been dubbed resonance-assisted hydrogen bonding (RAHB) and plays a major role in the energetics of the tautomeric equilibrium. The goal of this work was to investigate the role that pi-delocalization plays in the stability of RAHBs by engaging other isomerization processes. Similarly, acid-base chemistry has received little experimental attention in studies of RAHB, and we address the role that acid-base effects play in the tautomeric equilibrium. We find that pi-delocalization and the disruption of adjacent aromatic rings is the dominant effect in determining the stability of a RAHB.

We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 7467-91-6, and how the biochemistry of the body works.Application of 7467-91-6

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N128 | ChemSpider