59444-59-6

Basic information

• Product Name: Isoquinoline, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimeth oxy-
• CAS NO: 59444-59-6
• Molecular Formula: C20H24BrNO4
• Molecular Weight: 422.319
• Mol File: 59444-59-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Isoquinoline, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimeth oxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoquinoline, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimeth oxy-(59444-59-6)
• EPA Substance Registry System: Isoquinoline, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimeth oxy-(59444-59-6)

Safety Data

• Hazardous Substances Data: 59444-59-6(Hazardous Substances Data)

Upstream product

• 22185-91-7 2-(2-Bromo-4,5-dimethoxyphenyl)-N-<2-(3,4-dimethoxyphenyl)-ethyl>-acetamide 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 4697-57-8 methyl 2-(2-bromo-4,5-dimethoxyphenyl)acetate 
• 10313-60-7 3,4-dimethoxyphenylacetyl chloride 
• 4697-62-5 6-bromohomoveratric acid 
• 6831-57-8 2-bromo-4,5-dimethoxyphenylacetic acid chloride 
• 114105-51-0 N-(1-phenylethyl)-2-(3,4-dimethoxyphenyl)ethylamine 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 496817-65-3 n-[2-(2-bromo-4,5-dimethoxyphenyl)ethyl]-N-[(S)-1-phenylethyl]-2-(2-bromo-4,5-dimethoxyphenyl)acetamide 
• 496817-72-2 N-[2-(3,4-dimethoxyphenylethyl)]-N-(1-phenylethyl)-2-(2-bromo-4,5-dimethoxyphenyl)acetamide 
• 59444-56-3 1-(2'-bromo-4',5'-dimethoxybenzyl)-6,7-dimethoxy-3,4-dihydroisoquinoline hydrochloride 
• 53207-00-4 1-bromo-2-(bromomethyl)-4,5-dimethoxybenzene 
• 71783-57-8 methane sulfonate de dimethyoxy-6,7 dihydro-3,4 isoquinoleine 
• 41823-67-0 1-(2'-bromo-4',5'-dimethoxybenzyl)-6,7-dimethoxy-3,4-dihydroisoquinoline 

Downstream Products

• 1105064-59-2 C₄₇H₅₅BrN₂O₁₀ 
• 523-02-4 2,3,10,11-tetramethoxy-5,6,7,8,13,13a-hexahydroisoquinolino[3,2-a]isoquinoline 
• 6899-65-6 coralydine 
• 308818-03-3 1-[4',5'-dimethoxy-2'-(2-methylbutyryl)benzyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 3382-18-1 6,7-dimethoxy-3,4-dihydro-isoquinoline 
• 494-99-5 1,2-dimethoxy-4-methylbenzene 
• 124293-98-7 1-(2'-bromo-4',5'-dimethoxybenzyl)-2-ethoxycarbonyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Discovery of Aporphine Analogues as Potential Antiplatelet and Antioxidant Agents: Design, Synthesis, Structure–Activity Relationships, Biological Evaluations, and in silico Molecular Docking Studies

To explore the potential of aporphine alkaloids, a novel series of functionalized aporphine analogues with alkoxy (OCH3, OC2H5, OC3H7) functional groups at C1/C2 of ring A and an acyl (COCH3/sub

The palladium-catalyzed preparation of condensed tetracyclic heterocycles and their application to the synthesis of rac-mangochinine

Dihydroisoquinoline derivatives and their analogues, prepared by the Bischler-Napieralsky reaction, were converted to their indole-fused derivatives. Scope and limitations of the palladium-catalyzed reaction, proceeding through the tautomeric enamine forms of these compounds, were studied and the process was extended to the preparation of racemic mangochinine. Georg Thieme Verlag Stuttgart.

PHOTOCHEMICAL SYNTHESIS OF APORPHINES: (+/-)-GLAUCINE, (+/-)-NORGLAUCINE AND (+/-)-DEHYDRONORGLAUCINE

Photochemical cyclization of 3 afforded 5, 4 and 8. 5 on LAH reduction furnished (+/-)-glaucine (6) and on treatment with ethanolic HCl afforded (+/-)-norglaucine (7). 10 obtained by the photocyclization of 9 was converted into 7 and 11 via 12.