20341-16-6

Usage

Uses

Used in Pharmaceutical Industry:
N-[2-(1,3-benzodioxol-5-yl)ethyl]-2-(3,4-dimethoxyphenyl)acetamide is used as a potential therapeutic agent for various conditions due to its potential analgesic, anti-inflammatory, and psychoactive properties. Its structural similarity to certain neurotransmitters suggests that it may have applications in treating pain, inflammation, and possibly neurological or psychiatric disorders.
Used in Research and Development:
N-[2-(1,3-benzodioxol-5-yl)ethyl]-2-(3,4-dimethoxyphenyl)acetamide is used as a research compound to study its pharmacological effects and potential therapeutic applications. Further research is needed to understand its mechanism of action, efficacy, and safety profile, as well as to explore its potential use in drug development for various medical conditions.

Upstream product

• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 1484-85-1 3,4-methylenedioxyphenylethylamine 
• 10313-60-7 3,4-dimethoxyphenylacetyl chloride 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 68996-81-6 3-benzo[1,3]dioxol-5-yl-propionyl chloride 
• 2815-95-4 3-(1,3 benzodioxol-5-yl)propionic acid 
• 20799-84-2 3-(benzo[d][1,3]dioxol-5-yl)propanamide 
• 73663-57-7 (5-Benzo[1,3]dioxol-5-yl-oxazol-2-yl)-(3,4-dimethoxy-phenyl)-methanol 

Downstream Products

• 2221-44-5 5-(3,4-dimethoxy-benzyl)-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline 
• 19918-74-2 5-[(3,4-dimethoxyphenyl)methyl]-5,6,7,8-tetrahydro-1,3-dioxolo[4,5-g]isoquinoline 
• 81165-50-6 3-[5-(3,4-Dimethoxy-benzyl)-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-6-yl]-propionic acid 5-{3-[5-(3,4-dimethoxy-benzyl)-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-6-yl]-propionyloxy}-pentyl ester; compound with oxalic acid 
• 64229-26-1 C₄₈H₅₈N₂O₁₂⁽²⁺⁾*2I^(1-) 
• 64229-27-2 C₅₁H₆₄N₂O₁₂⁽²⁺⁾*2I^(1-) 
• 81165-49-3 3-[5-(3,4-Dimethoxy-benzyl)-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-6-yl]-propionic acid 2-{3-[5-(3,4-dimethoxy-benzyl)-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-6-yl]-propionyloxy}-ethyl ester; compound with oxalic acid 
• 20341-48-4 (7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-(3,4-dimethoxy-phenyl)-methanone 

Relevant academic research and scientific papers

Oxazoles in Organic Chemistry. 2. Application to the Synthesis of Benzylisoquinoline Alkaloids

A conceptually new route to the benzylisoquinoline alkaloids has been devised.The reaction of 2-lithiooxazoles with aromatic aldehydes to generate the thermodynamically favored 2-substituted oxazoles constitutes the key step in this process.A single-pot two carbon-carbon bond-joining reaction leading to an oxazoline suitable for further transformation to a phenethylamide is also described.