23818-68-0

Basic information

• Product Name: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-phenylisoquinoline
• Synonyms: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-phenylisoquinoline
• CAS NO: 23818-68-0
• Molecular Weight: 423.533
• Mol File: 23818-68-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-phenylisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-phenylisoquinoline(23818-68-0)
• EPA Substance Registry System: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-phenylisoquinoline(23818-68-0)

Safety Data

• Hazardous Substances Data: 23818-68-0(Hazardous Substances Data)

Upstream product

• 14165-67-4 N-(3,4-dimethoxyphenethyl)-4-methylbenzenesulfonamide 
• 100-52-7 benzaldehyde 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 4118-36-9 6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline 

Downstream Products

• 4029-09-8 6,7-dimethoxy-1-phenyl-isoquinoline 
• 1256550-21-6 1-phenyl-2-tosyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol 
• 1256550-22-7 C₂₂H₁₉NO₄S 
• 1256550-25-0 7-fluoro-1-phenyl-2-tosyl-1,2,3,4-tetrahydroisoquinolin-6-ol 
• 1256550-26-1 6-fluoro-1-phenyl-2-tosyl-1,2,3,4-tetrahydroisoquinolin-6-ol 
• 10172-51-7 6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinoline 

Relevant articles and documents

Synthesis, cytotoxicity and QSAR study of N-tosyl-1,2,3,4- tetrahydroisoquinoline derivatives

1-Substituted-N-tosyl-1,2,3,4-tetrahydroisoquinoline analogs (4a-4l) were synthesized using the modified Pictet-Spengler reaction and evaluated for cytotoxicity. All tetrahydroisoquinolines displayed cytotoxicity against MOLT-3 cell lines, except for p-me

Nucleophilic deoxyfluorination of catechols

Nucleophilic deoxyfluorinaiton of one of the two hydroxyl groups of catechols has been developed via the Umpolung concept. This method was successively applied to naturally occurring catechols, such as catechins and dopamine, to produce novel fluorinated

Thiophenol-mediated improvement of the Pictet-Spengler cyclization of N-tosyl-β-phenethylamines with aldehydes

The Lewis acid-catalyzed Pictet-Spengler condensation of N-tosyl-β-phenethylamines with aldehydes is improved by the addition of thiophenol, furnishing better yields of 1-substituted tetrahydroisoquinolines at a given time.