91586-47-9

Basic information

• Product Name: 7-Acetoxy-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline
• Synonyms: 7-Acetoxy-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline
• CAS NO: 91586-47-9
• Molecular Weight: 355.39
• Mol File: 91586-47-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-Acetoxy-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Acetoxy-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline(91586-47-9)
• EPA Substance Registry System: 7-Acetoxy-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline(91586-47-9)

Safety Data

• Hazardous Substances Data: 91586-47-9(Hazardous Substances Data)

Upstream product

• 91586-44-6 7-Acetyl-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline 
• 91586-26-4 1-(4-methoxybenzoyl)piperidin-4-one 
• 190012-08-9 1-(4-methoxybenzoyl)-4-piperidone ethylene ketal 
• 91586-29-7 Methyl 6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylate 
• 91586-46-8 6-Methoxy-2-(4-methoxy-benzoyl)-1,2,3,4-tetrahydro-isoquinoline-7-carbonyl chloride 
• 91586-45-7 6-Methoxy-2-(4-methoxy-benzoyl)-1,2,3,4-tetrahydro-isoquinoline-7-carboxylic acid 
• 91586-27-5 6-(4-Methoxy-benzoyl)-2-oxo-5,6,7,8-tetrahydro-2H-pyrano[3,2-c]pyridine-3-carboxylic acid methyl ester 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 5056-80-4 (+/-)-sendaverine 

Relevant articles and documents

Inverse Electron Demand Diels-Alder Reactions of 3-Carbomethoxy-2-pyrones. Controlled Introduction of Oxygenated Aromatics: Benzene, Phenol, Catechol, Resorcinol, and Pyrogallol Annulation. Regiospecific Total Synthesis of Sendaverine and a Preparation of 6,7-Benzomorphans

A full investigation of the preparation and Diels-Alder reactions of 3-carbomethoxy-2-pyrones is described.Methods for the preparation of a full range of oxygen-substituted aromatics: benzene, 1-, 2-, or 3-phenol, symmetrical or unsymmetrical o-catechol, resorcinol, and pyrogallol annulation from a common 3-carbomethoxy-2-pyrone intermediate are detailed.A regiospecific total synthesis of sendaverine, a 2-benzyltetrahydroisoquinoline possessing a selectively protected, symmetrical o-catechol, and a preparation of 6,7-benzomorphans are described.