Properties and Exciting Facts About 7-Amino-1,8-naphthyridin-2(8H)-one

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 1931-44-8

Synthetic Route of 1931-44-8, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1931-44-8, Name is 7-Amino-1,8-naphthyridin-2(8H)-one, molecular formula is C8H7N3O. In a Patent£¬once mentioned of 1931-44-8

Rhone-Poulenc Industries

Heterocyclic compounds of the formula: STR1 wherein the pyrroline ring and the symbols X1 and X2 together form an unsubstituted or substituted isoindoline nucleus, or a 6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine, 6,7-dihydro-5H-pyrrolo[3,4-b]pyridine or 2,3,6,7-tetrahydro-5H-1,4-oxathiino[2,3-c]pyrrole nucleus, the 1,8-naphthyridin-2-yl nucleus is unsubstituted or substituted, and the grouping –NR1 R2 is an amino or substituted amino group, are new compounds which are active as tranquillizers, hypnotics, anti-convulsant agents and anti-spasmodics.

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 1931-44-8

Reference£º
1,446-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N440 – PubChem