158587-31-6

Basic information

• Product Name: (+/-)-(4RS)-4-(4-bromophenyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline
• CAS NO: 158587-31-6
• Molecular Weight: 302.214
• Mol File: 158587-31-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+/-)-(4RS)-4-(4-bromophenyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-(4RS)-4-(4-bromophenyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline(158587-31-6)
• EPA Substance Registry System: (+/-)-(4RS)-4-(4-bromophenyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline(158587-31-6)

Safety Data

• Hazardous Substances Data: 158587-31-6(Hazardous Substances Data)

Upstream product

• 1431664-66-2 C₁₀H₁₂BrNO 
• 103-67-3 benzyl-methyl-amine 
• 6291-68-5 2-(benzyl(methyl)amino)-1-(4'-bromophenyl)ethanone hydrochloride 
• 133961-99-6 1-(4-bromophenyl)-2-<(N-benzyl-N-methyl)amino>-ethanol 
• 32017-76-8 (+/-)-2-(4-bromophenyl)oxirane 
• 99-73-0 para-bromophenacyl bromide 

Relevant articles and documents

Synthesis of 6,12-Methanodibenzo[ c, f]azocines and 4-Aryltetrahydroisoquinolines from Aromatic Aldehydes

A methodology for the synthesis of 7,12-dihydro-5H-6,12-methanodibenzo[c,f]azocines from aromatic aldehydes and N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine using catalysis by trifluoroacetic and perchloric acids is described. The developed protocol was applied for the synthesis of N-unsubstituted and N-methyl-4-aryltetrahydroisoquinolines.

Synthesis, antiulcer and antidepressive activity of 4-(4-halophenyl)-2-phenyl-1,2,3,4-tetrahydroisoquinolines

4-(4-halophenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinolines 2a-c have been synthesized by two methods and their biochemical and pharmacological properties have been studied. Biochemical investigations showed that all the compounds are strong inhibitors of