Brief introduction of 6-Methyl-1,2,3,4-tetrahydroisoquinoline

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 42923-76-2

Electric Literature of 42923-76-2, 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.42923-76-2, Name is 6-Methyl-1,2,3,4-tetrahydroisoquinoline, molecular formula is C10H13N. In a article£¬once mentioned of 42923-76-2

6-substituted-1,2,3,4-tetrahydroisoquinolines

Compounds of the formula: STR1 wherein n=1 or 2; R 1 is lower alkoxy, lower alkyl, halo, ester, carbamate, or substituted amino; and R 2 is thienyl or furyl; or R 2 is STR2 wherein R 3 and R 4 are independently selected from hydrogen, halo, hydroxy, methoxy, thioalkoxy, substituted amino and lower alkyl; and pharmaceutically acceptable salts thereof.These compounds are useful as inhibitors of alpha-2-adrenergic receptors and for the treatment of glaucoma and/or controlling intraocular pressure.

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 42923-76-2

Reference£º
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem