83287-04-1

Basic information

• Product Name: Benzoic acid, 2-(6,7-dimethoxy-1-isoquinolinyl)-5-methoxy-
• CAS NO: 83287-04-1
• Molecular Formula: C19H17NO5
• Molecular Weight: 339.348
• Mol File: 83287-04-1.mol

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-(6,7-dimethoxy-1-isoquinolinyl)-5-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-(6,7-dimethoxy-1-isoquinolinyl)-5-methoxy-(83287-04-1)
• EPA Substance Registry System: Benzoic acid, 2-(6,7-dimethoxy-1-isoquinolinyl)-5-methoxy-(83287-04-1)

Safety Data

• Hazardous Substances Data: 83287-04-1(Hazardous Substances Data)

Upstream product

• 15547-67-8 6,7-dimethoxy-1-(4-methoxy-phenyl)-isoquinoline 
• 1013931-27-5 1-Iodo-6,7-dimethoxyisoquinoline 
• 15248-39-2 6,7-dimethoxyisoquinoline 
• 88741-65-5 methyl 2-(6,7-dimethoxyisoquinolin-1-yl)-5-methoxybenzoate 
• 88741-40-6 2-Brom-4-methoxybenzoesaurechlorid 
• 4722-08-1 3,4-dimethoxy-β-methoxybenzeneethanamine 
• 83287-07-4 N-(3',4',β-trimethoxyphenethyl)-2-bromo-4-methoxybenzamide 
• 83287-05-2 2-(6,7-dimethoxy-isoquinolin-1-yl)-5-methoxybenzonitrile 

Downstream Products

• 83287-02-9 menisporphine 
• 88741-65-5 methyl 2-(6,7-dimethoxyisoquinolin-1-yl)-5-methoxybenzoate 

Relevant articles and documents

Ni-Catalyzed C-H Cyanation of (Hetero)arenes with 2-Cyanoisothiazolidine 1,1-Dioxide as a Cyanation Reagent

A nickel-catalyzed C-H cyanation reaction of arenes has been developed using 2-cyanoisothiazolidine 1,1-dioxide as an electrophilic cyanation reagent. Many different directing groups can be used in this cyanation to obtain a series of cyanation products with good yields. Adopting this strategy to introduce a cyano group, natural alkaloid menisporphine was successfully synthesized through cyano group conversion that further proved the practicality of this cyanation method.

A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines

Oxoisoaporphine alkaloids are conveniently prepared via direct ring metalation of alkoxy-substituted isoquinolines at C-1, followed by reaction with iodine. Subsequent Suzuki cross-coupling of the resulting 1-iodoisoquinolines to methyl 2-(isoquinolin-1-y

STRUCTURE AND SYNTHESIS OF MENISPORPHINE, A NEW TYPE OF ISOQUINOLINE ALKALOID. ALKALOIDS OF MENISPERMUM DAURICUM DC. (9)

The structure of an unknown yellow base from Menispermum dauricum DC. (Menispermaceae) was determined to be 5,6,9-trimethoxy-7H-dibenzoquinolin-7-one from various spectral data and synthesis, and was named menisporphine.This is a new isoquinoline-ty