65899-28-7

Basic information

• Product Name: Isoquinoline, 1-[2-(3,4-dimethoxyphenyl)ethyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-
• CAS NO: 65899-28-7
• Molecular Formula: C21H27NO4
• Molecular Weight: 357.45
• Mol File: 65899-28-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Isoquinoline, 1-[2-(3,4-dimethoxyphenyl)ethyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoquinoline, 1-[2-(3,4-dimethoxyphenyl)ethyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-(65899-28-7)
• EPA Substance Registry System: Isoquinoline, 1-[2-(3,4-dimethoxyphenyl)ethyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-(65899-28-7)

Safety Data

• Hazardous Substances Data: 65899-28-7(Hazardous Substances Data)

Upstream product

• 3382-18-1 6,7-dimethoxy-3,4-dihydro-isoquinoline 
• 40173-90-8 3,4-dimethoxyphenethyl bromide 
• 2107-70-2 3,4-methoxycinnamic acid 
• 20944-13-2 N-<2-(3,4-dimethoxyphenyl)ethyl>-3-(3,4-dimethoxyphenyl)propionamide 
• 20944-14-3 1-[2-(3,4-dimethoxyphenyl)-ethyl]-6,7-dimethoxy-3,4-dihydroisoquinoline 
• 2859-78-1 4-Bromoveratrole 
• 933067-43-7 1,2-dimethoxy-4-prop-2-ynyl-benzene 
• 79631-01-9 1,2-dimethoxy-4-<1-<(1,1-dimethylethyl)dimethylsilyloxy>ethenyl>benzene 
• 123190-12-5 2-(2-bromoethyl)-4,5-(dimethoxy)benzaldehyde 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 

Downstream Products

• 32487-03-9 6,7-dimethoxy-1-(3,4-dimethoxyphenylethyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline 
• 758711-93-2 2-(2-(2-Chloro-5-nitro-phenoxy)-ethyl)-1-(2-(3,4-dimethoxy-phenyl)-ethyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline 
• 81182-05-0 1,13-bis-<1,2,3,4-tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)ethyl>-isoquinolin-2-yl>-4,10-dioxa-3,11-dioxotridecane dioxalate 

Relevant articles and documents

ANTI-HIV COMPOUNDS

This invention provides, among other things, tetrahydroisoquinolines useful for treating viral infections, pharmaceutical formulations containing such compounds, as well as methods of inhibiting the replication of a virus, such as HIV, or treating a disease, such as AIDS.

Unified approach to isoindolinones and THIQs via lewis acid catalyzed domino mukaiyama-mannich Lactamization/Alkylations: Application in the synthesis of (±)-homolaudanosine

A novel and efficient synthesis of a variety of isoindolinones and tetrahydroisoquinolines via a Lewis acid catalyzed domino Mukaiyama-Mannich lactamization/alkylation is achieved. This transformation comprises a sequential formation of three new bonds through a one-pot, three-component procedure to afford product in moderate to high yields. A concise synthesis of (±)-homolaudanosine (2b) has been achieved using this method.

TETRAHYDROISOQUINOLYL ACETAMIDE DERIVATIVES FOR USE AS OREXIN RECEPTOR ANTAGONISTS

The invention relates to novel acetamide derivatives of formula (I) and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of such compound