100710-88-1

Basic information

• Product Name: 2-(3,4-dimethoxybenzyl)pyridine
• Synonyms: 2-(3,4-dimethoxybenzyl)pyridine
• CAS NO: 100710-88-1
• Molecular Weight: 229.279
• Mol File: 100710-88-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(3,4-dimethoxybenzyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-dimethoxybenzyl)pyridine(100710-88-1)
• EPA Substance Registry System: 2-(3,4-dimethoxybenzyl)pyridine(100710-88-1)

Safety Data

• Hazardous Substances Data: 100710-88-1(Hazardous Substances Data)

Upstream product

• 21852-32-4 4-bromomethyl-1,2-dimethoxybenzene 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 100-70-9 2-Cyanopyridine 
• 1699-51-0 laudanosine 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 109-09-1 2-chloropyridine 
• 5005-41-4 3,4-dimethoxyphenyl-(2-pyridyl)acetonitrile 
• 31749-10-7 (3,4-dimethoxyphenyl)(pyridin-2-yl)methanol 

Downstream Products

• 33455-70-8 N-methyl-2-(3,4-dimethoxybenzyl)piperidine 
• 108958-45-8 N-n.propyl-2-(3,4-dimethoxybenzyl)piperidine 
• 108958-39-0 N-acetyl-2-(3,4-dimethoxybenzyl)piperidine 
• 108958-41-4 N-propionyl-2-(3,4-dimethoxybenzyl)piperidine 
• 108997-38-2 N-ethoxycarbonyl-2-(3,4-dimethoxybenzyl)piperidine 
• 108958-44-7 N-ethyl-2-(3,4-dimethoxybenzyl)piperidine 
• 6495-96-1 8,9-dimethoxy-4,6,11,11a-tetrahydro-1H-benzoquinolizine 
• 109728-33-8 1-acetonyl-2-veratryl-pyridinium; iodide 
• 102458-70-8 2-(3,4-dimethoxybenzyl)piperidine 
• 112578-50-4 1-phenacyl-2-veratryl-pyridinium; bromide 

Relevant articles and documents

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.

Interaction of some 2-hydroxybenzylpiperidines with dopamine receptors

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