787571-92-0

Basic information

• Product Name: N-(3,5-dimethyl-4-hydroxyphenethyl)-N-tosyl-3,4-dimethoxybenzylamine
• CAS NO: 787571-92-0
• Molecular Weight: 469.602
• Mol File: 787571-92-0.mol

Chemical Properties

• CAS DataBase Reference: N-(3,5-dimethyl-4-hydroxyphenethyl)-N-tosyl-3,4-dimethoxybenzylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,5-dimethyl-4-hydroxyphenethyl)-N-tosyl-3,4-dimethoxybenzylamine(787571-92-0)
• EPA Substance Registry System: N-(3,5-dimethyl-4-hydroxyphenethyl)-N-tosyl-3,4-dimethoxybenzylamine(787571-92-0)

Safety Data

• Hazardous Substances Data: 787571-92-0(Hazardous Substances Data)

Upstream product

• 787571-86-2 methyl 4-benzyloxy-3,5-dimethylphenylacetate 
• 787571-87-3 2-(4-benzyloxy-3,5-dimethyl-phenyl)-ethanol 
• 787571-88-4 4-benzyloxy-3,5-dimethylphenethyl bromide 
• 168106-30-7 3,5-dimethyl-4-benzyloxy-phenyl acetic acid 
• 787571-89-5 N-(4-benzyloxy-3,5-dimethylphenethyl)-N-tosyl-3,4-dimethoxybenzylamine 

Downstream Products

• 787571-95-3 N-(3,4-dimethoxy-benzyl)-N-[2-(3,5-dimethyl-4-oxo-cyclohexa-2,5-dienylidene)-ethyl]-4-methyl-benzenesulfonamide 

Relevant articles and documents

Quinone methide initiated cyclization reaction: Synthesis of 4-aryl-1,2,3,4-tetrahydroisoquinolines

4-Aryl-1,2,3,4-tetrahydroisoquinolines were synthesized in very good yields by in situ generation of p-quinone methides resulting in a novel C-C bond cyclization. 4-Aryl-1,2,3,4-tetrahydroisoquinolines were synthesized in very good yields by in situ gener