21965-92-4

Basic information

• Product Name: Isoquinoline, 1-[(3,4-dimethoxyphenyl)methyl]-
• CAS NO: 21965-92-4
• Molecular Formula: C18H17NO2
• Molecular Weight: 279.338
• Mol File: 21965-92-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Isoquinoline, 1-[(3,4-dimethoxyphenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoquinoline, 1-[(3,4-dimethoxyphenyl)methyl]-(21965-92-4)
• EPA Substance Registry System: Isoquinoline, 1-[(3,4-dimethoxyphenyl)methyl]-(21965-92-4)

Safety Data

• Hazardous Substances Data: 21965-92-4(Hazardous Substances Data)

Upstream product

• 2024-83-1 veratronitrile 
• 2859-58-7 1,2-dihydroisoquinoline 
• 88422-82-6 1-(3',4'-dimethoxybenzyl)-3,4-dihydroisoquinoline 
• 1374461-31-0 N-methoxy 1-(4-methoxybenzyl)isoquinolinium perchlorate 
• 1374461-33-2 N-methoxy 1-(3,4-dimethoxybenzyl)isoquinolinium perchlorate 
• 23974-81-4 1-(4-methoxybenzyl)isoquinoline N-oxide 
• 1198-30-7 1-isoquinolinecarbonitrile 
• 1699-51-0 laudanosine 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 21852-32-4 4-bromomethyl-1,2-dimethoxybenzene 
• 119-65-3 isoquinoline 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 7306-46-9 4-chloromethyl-1,2-dimethoxy-benzene 
• 107779-30-6 (3,4-dimethoxy-phenyl)-acetic acid-(2-cyclohexa-1,4-dienyl-ethylamide) 

Downstream Products

• 98237-20-8 1-(3,4-Dimethoxybenzyl)-5,6,7,8-tetrahydroisochinolin 
• 22988-16-5 1-(3',4'-dimethoxybenzyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline 
• 50370-93-9 1-(3',4'-dimethoxybenzyl)-2-methylisoquinolinium iodide 

Relevant articles and documents

Visible Light-Mediated Direct Decarboxylative C-H Functionalization of Heteroarenes

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Transition-Metal-Free Decarboxylative Photoredox Coupling of Carboxylic Acids and Alcohols with Aromatic Nitriles

A transition-metal-free protocol for the redox-neutral light-induced decarboxylative coupling of carboxylic acids with (hetero)aromatic nitriles at ambient temperature is presented. A broad scope of acids and nitriles is accepted, and alcohols can be coupled in a similar fashion through their oxalate half esters. Various inexpensive sources of UV light and even sunlight can be used to achieve this C-C bond formation proceeding through a free radical mechanism.