In 1968,Chemical & Pharmaceutical Bulletin included an article by Tachibana, Shinro; Matsuo, Hisayuki; Yamada, Shunichi. SDS of cas: 54329-54-3. The article was titled 《Chemistry of amino acids. IV. Decarboxylation of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid and its derivatives》. The information in the text is summarized as follows:
Decarboxylation of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives, I, II, III, IV and IV.HCl, in acetophenone and BzH solvents, was examined In the case of IV.HCl, 4-substituted isoquinoline derivatives were formed in moderate yield according to the solvent used. 25 references. After reading the article, we found that the author used 2-Methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid(cas: 54329-54-3SDS of cas: 54329-54-3)
2-Methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid(cas: 54329-54-3) belongs to tetrahydroisoquinoline. Tetrahydroisoquinoline Reactions: As a secondary amine, tetrahydroisoquinoline has weakly basic properties and forms salts with strong acids.SDS of cas: 54329-54-3 It can be dehydrogenated to give isoquinoline and hydrogenated to decahydroisoquinoline. Like other secondary amines, tetrahydroisoquinoline can be oxidized to the corresponding nitrone using hydrogen peroxide, catalyzed by selenium dioxide.
Referemce:
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem