Chemical Properties and Facts of Methyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.SDS of cas: 57060-88-5, you can also check out more blogs about57060-88-5

Research speed reading in 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. An article , which mentions SDS of cas: 57060-88-5, molecular formula is C11H14ClNO2. The compound – Methyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride played an important role in people’s production and life., SDS of cas: 57060-88-5

Compounds of the general formula: STR1 wherein: the ring A is saturated and n=0 or 1, or the ring A is a benzene ring and n=1, R1 represents a lower alkyl group which can carry an amino group, R2 represents a hydrogen atom or a lower alkyl group, R3 represents a straight or branched alkyl group, a mono- or di-cycloalkylalkyl or phenylalkyl group having no more than a total of 9 carbon atoms, or a substituted alkyl group, and also the salts thereof. These compounds are useful as therapeutic drugs.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.SDS of cas: 57060-88-5, you can also check out more blogs about57060-88-5

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