25200-15-1

Basic information

• Product Name: 6-hydroxy-1-phenyl-1,2,3,4-tetrahydro-isoquinoline
• Synonyms: 6-hydroxy-1-phenyl-1,2,3,4-tetrahydro-isoquinoline
• CAS NO: 25200-15-1
• Molecular Weight: 225.29
• Mol File: 25200-15-1.mol

Chemical Properties

• CAS DataBase Reference: 6-hydroxy-1-phenyl-1,2,3,4-tetrahydro-isoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-hydroxy-1-phenyl-1,2,3,4-tetrahydro-isoquinoline(25200-15-1)
• EPA Substance Registry System: 6-hydroxy-1-phenyl-1,2,3,4-tetrahydro-isoquinoline(25200-15-1)

Safety Data

• Hazardous Substances Data: 25200-15-1(Hazardous Substances Data)

Upstream product

• 347979-10-6 2,2,2-Trifluoro-1-(6-hydroxy-1-phenyl-3,4-dihydro-1H-isoquinolin-2-yl)ethanone 
• 2039-67-0 2-(3-methoxyphenyl)-1-ethanamine 
• 588-05-6 m-tyramine 
• 100-52-7 benzaldehyde 

Relevant articles and documents

Regioselective bromination of 6-hydroxytetrahydroisoquinolines

Regioselective bromination of 6-hydroxytetrahydroisoquinolines using molecular bromine was disclosed. Treatment of 6-hydroxytetrahydroisoquinolines with molecular bromine under different temperatures afforded 5-bromo-6-hydroxytetrahydroisoquinolines as so

1-Aryl-1,2,3,4-tetrahydroisoquinolines as potential antimalarials: Synthesis, in vitro antiplasmodial activity and in silico pharmacokinetics evaluation

In the present study, twenty-one 1-aryl-6-hydroxy-1,2,3,4- tetrahydroisoquinoline (THIQ) analogues were synthesized by base-catalyzed Pictet-Spengler reaction, and tested in vitro against P. falciparum using the [3H]hypoxanthine incorporation a

Calcium-catalyzed pictet-spengler reactions

(Chemical Equation Presented) Pictet-Spengler reactions of m-tyramine and aldehydes produced tetrahydroisoquinolines in the presence of a catalytic amount of Ca[OCH(CF3)2]2. This reaction occurs with a variety of aryl, het

Catalytic Pictet-Spengler reactions using Yb(OTf)3

The catalytic Pictet-Spengler reactions proceeded in high yields with high regioselectivity in the presence of a catalytic amount of Yb(OTf)3 and a dehydrating agent at room temperature. High regioselectivities were obtained in these reactions,