57010-78-3

Basic information

• Product Name: N-[3-(3,4-DIMETHOXYPHENYL)PROPYL]-N-METHYLAMINE
• Synonyms: 3-(3,4-Dimethoxyphenyl)-N-methylpropan-1-amine
• CAS NO: 57010-78-3
• Molecular Formula: C₁₂H₁₉NO₂
• Molecular Weight: 209.28
• Mol File: 57010-78-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 304.2°Cat760mmHg
• Flash Point: 126°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.000889mmHg at 25°C
• Refractive Index: 1.496
• CAS DataBase Reference: N-[3-(3,4-DIMETHOXYPHENYL)PROPYL]-N-METHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-[3-(3,4-DIMETHOXYPHENYL)PROPYL]-N-METHYLAMINE(57010-78-3)
• EPA Substance Registry System: N-[3-(3,4-DIMETHOXYPHENYL)PROPYL]-N-METHYLAMINE(57010-78-3)

Safety Data

• Hazardous Substances Data: 57010-78-3(Hazardous Substances Data)

Usage

Description

N-[3-(3,4-Dimethoxyphenyl)propyl]-N-methylamine is a chemical compound characterized by the molecular formula C13H21NO2. It is a tertiary amine with a propyl chain that features a 3,4-dimethoxyphenyl group and a methyl group. N-[3-(3,4-DIMETHOXYPHENYL)PROPYL]-N-METHYLAMINE is recognized for its potential in pharmaceutical research and drug development, serving as a versatile building block for the synthesis of a variety of organic compounds. Its pharmacological properties have been a subject of study, making it a compound of interest in medicinal chemistry. Furthermore, it holds promise for applications in organic synthesis for the creation of diverse functional materials.

Uses

Used in Pharmaceutical Research and Drug Development:
N-[3-(3,4-DIMETHOXYPHENYL)PROPYL]-N-METHYLAMINE is used as a building block for the synthesis of various organic compounds, playing a crucial role in the development of new pharmaceutical agents. Its unique structure allows for the creation of molecules with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, N-[3-(3,4-DIMETHOXYPHENYL)PROPYL]-N-METHYLAMINE is used as a precursor for the production of various functional materials. Its chemical properties enable the synthesis of compounds with tailored characteristics for specific applications, broadening its utility in material science and related industries.

InChI:InChI=1/C12H19NO2/c1-13-8-4-5-10-6-7-11(14-2)12(9-10)15-3/h6-7,9,13H,4-5,8H2,1-3H3

Upstream product

• 14773-42-3 3-(3,4-dimethoxyphenyl)propylamine 
• 115032-14-9 [3-(3,4-Dimethoxy-phenyl)-propyl]-[1-phenyl-meth-(E)-ylidene]-amine 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1070775-15-3 C₂₉H₃₃NO₁₀S 
• 92460-18-9 1-[7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(3-{3,4-dimethoxy-phenyl}-propyl)-amino]-propane hydrochloride 
• 115032-17-2 N-<3-(3,4-Dimethoxyphenyl)propyl>-N-methylbenzylamin 
• 115032-10-5 N-<3-(3,4-Dimethoxyphenyl)propyl>-N-methylbenzylamin-hydrochlorid 
• 115032-09-2 N-<3-(3,4-Dimethoxyphenyl)propyl>-N-methylbenzamid 

Relevant articles and documents

Isoquinobenzazepines, II. - Preparation of 1-Phenyl-2-benzazepine Derivatives by Bischler-Napieralski Reaction

Starting with N-(3-Phenylpropyl)benzamides 2, the possibilities and limits of the Bischler-Napieralski reaction leading to a sevenmembered ring have been systematically studied.We found that cyclisation is only observed when the amide is activated and cap