Chemical Properties and Facts of 217192-22-8

Although many compounds look similar to this compound(217192-22-8)Application In Synthesis of (4-(Pyridin-4-yl)phenyl)methanol, numerous studies have shown that this compound(SMILES:OCC1=CC=C(C2=CC=NC=C2)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Application In Synthesis of (4-(Pyridin-4-yl)phenyl)methanol. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (4-(Pyridin-4-yl)phenyl)methanol, is researched, Molecular C12H11NO, CAS is 217192-22-8, about Aerobic Oxidation of Alcohols and the Synthesis of Benzoxazoles Catalyzed by a Cuprocupric Coordination Polymer (Cu+-CP) Assisted by TEMPO. Author is Feng, Xun; Xu, Chen; Wang, Zhi-Qiang; Tang, Si-Fu; Fu, Wei-Jun; Ji, Bao-Ming; Wang, Li-Ya.

A Cu+-coordination polymer (CP) based on the tetranuclear unit {[(HSQPA)2Cu4(bipy)4]·2H2O}n·2nH2O was constructed through Cu2+ salt, 2-(sulfonylquinolin-8-yloxy)phthalic acid (H3SQPA), and 4,4′-bipyridine (bipy). This Cu+-CP combined with 2,2,6,6-tetramethylpiperidine-1-oxyl as the cocatalyst is an effective catalyst for aerobic oxidation of alcs. and the synthesis of benzoxazoles and can be recycled at least four times without losing its catalytic activity.

Although many compounds look similar to this compound(217192-22-8)Application In Synthesis of (4-(Pyridin-4-yl)phenyl)methanol, numerous studies have shown that this compound(SMILES:OCC1=CC=C(C2=CC=NC=C2)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider