110011-00-2

Basic information

• Product Name: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-(4-nitrophenyl)isoquinoline
• Synonyms: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-(4-nitrophenyl)isoquinoline
• CAS NO: 110011-00-2
• Molecular Weight: 468.53
• Mol File: 110011-00-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-(4-nitrophenyl)isoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-(4-nitrophenyl)isoquinoline(110011-00-2)
• EPA Substance Registry System: 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1-(4-nitrophenyl)isoquinoline(110011-00-2)

Safety Data

• Hazardous Substances Data: 110011-00-2(Hazardous Substances Data)

Upstream product

• 14165-67-4 N-(3,4-dimethoxyphenethyl)-4-methylbenzenesulfonamide 
• 555-16-8 4-nitrobenzaldehdye 

Relevant articles and documents

Tungstophosphoric acid catalyzed synthesis of N-sulfonyl-1,2,3,4- tetrahydroisoquinoline analogs

An operationally simple and eco-friendly protocol has been developed for the synthesis of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines 3 using the modified Pictet-Spengler reaction of N-sulfonylphenylethylamines 1 and various aldehydes 2 in the presence of

Application of the Intramolecular α-Aminoalkylation Reaction for the Synthesis of 2-Arylsulfonyl-1,2,3,4-tetrahydroisoquinolines

The adducts of azomethines and sulfonyl chlorides (Method A) as well as hydroxymethylated sulfonamides (Method B) are used for the synthesis of 2-arylsulfonyl-1,2,3,4-tetrahydroisoquinolines 4a-q.