Reference of 64175-51-5, 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.64175-51-5, Name is 2-(Benzofuran-3-yl)acetic acid, molecular formula is C10H8O3. In a article£¬once mentioned of 64175-51-5
Condensed pyridine bases. Synthesis and reactions of benzofuro[2,3-c] indeno[2,1-e]-, benzothieno[2,3-c]indeno[2,1-e]-, benzofuro-[3,2-c]indeno[2,1-e] – and thieno[2,3:4?,5?]-thieno[3,2-c]indeno[2,1-e]pyridines
Condensation of hetarene carboxaldehydes with phthalide gave 2-(3-hydroxy-1-oxoinden-2-yl)benzo[b]furan and 2-(3-hydroxy-1-oxoinden-2-yl)-5- ethylthieno[2,3-b]thiophene. Starting from hetaryl acetic acids gave 3-(3-hydroxy-1-oxoinden-2-yl)benzo[b]furan and 3-(3-hydroxy-1-oxoinden-2-yl) benzo[b]thiophene. Acylation of 3-hydroxy-1-oxoinden-2-yl-substituted heterocycles using acetic anhydride in the presence of 70% HClO4 leads to the formation of pentacyclic pyrilium salts. Pentacyclic indenopyridines are prepared by treating the pyrilium salts with ammonia. The reaction of the carbonyl group in the indenopyridines with hydroxylamine, hydrazine hydrate, and in reduction using NaBH4 has been studied.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 64175-51-5
Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H2680O – PubChem