19713-28-1

Basic information

• Product Name: 2-(3,4-dimethoxyphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]ethanaminium chloride
• CAS NO: 19713-28-1
• Molecular Formula: C₂₀H₂₇NO₄*ClH
• Molecular Weight: 381.8936
• Mol File: 19713-28-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 472.5°C at 760 mmHg
• Flash Point: 203.9°C
• Vapor Pressure: 4.26E-09mmHg at 25°C
• CAS DataBase Reference: 2-(3,4-dimethoxyphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]ethanaminium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4-dimethoxyphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]ethanaminium chloride(19713-28-1)
• EPA Substance Registry System: 2-(3,4-dimethoxyphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]ethanaminium chloride(19713-28-1)

Safety Data

• Hazardous Substances Data: 19713-28-1(Hazardous Substances Data)

Usage

Compound type

Quaternary ammonium compound

Structure

Two 3,4-dimethoxyphenyl groups attached to a central ethanamine structure

Usage

Organic synthesis, pharmaceutical research, potential applications in medicine and drug development

Unique features

Valuable for scientific and industrial purposes due to its structure and properties

Upstream product

• 139-76-4 N-(3,4-dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)acetamide 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 40173-90-8 3,4-dimethoxyphenethyl bromide 

Relevant articles and documents

Oxidative Coupling of Phenols and Phenolic Ethers. Part 4. Synthesis of Dibenzazonines and a Dibenzazecine, via Direct Coupling

Two series of amides, N-phenethylphenylacetamides (9) and the bisphenetylamides (11), including diphenolic monophenolic, and non-phenolic types, were treated with a range of one-electron oxidants.With the tetramethoxy-derivative (11e) intramolecular coupling yielded a dibenzazonine (16) in 36percent yield.Similar oxidation of the homologue (18) gave a dibenzazecine (19) in 60percent yield.