174661-97-3

Basic information

• Product Name: 2-[4-(2-aminoethoxy)-3-methoxyphenyl]-N-[3-(3,4-dimethylphenyl)propyl]acetamide hydrochloride (1:1)
• CAS NO: 174661-97-3
• Molecular Formula: C₂₂H₃₀N₂O₃*ClH
• Molecular Weight: 406.9461
• Mol File: 174661-97-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 594.6°C at 760 mmHg
• Flash Point: 313.4°C
• Vapor Pressure: 4.16E-14mmHg at 25°C
• CAS DataBase Reference: 2-[4-(2-aminoethoxy)-3-methoxyphenyl]-N-[3-(3,4-dimethylphenyl)propyl]acetamide hydrochloride (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[4-(2-aminoethoxy)-3-methoxyphenyl]-N-[3-(3,4-dimethylphenyl)propyl]acetamide hydrochloride (1:1)(174661-97-3)
• EPA Substance Registry System: 2-[4-(2-aminoethoxy)-3-methoxyphenyl]-N-[3-(3,4-dimethylphenyl)propyl]acetamide hydrochloride (1:1)(174661-97-3)

Safety Data

• Hazardous Substances Data: 174661-97-3(Hazardous Substances Data)

Upstream product

• 147497-64-1 DA-5018 

Downstream Products

• 147497-64-1 DA-5018 

Relevant articles and documents

CATALYTIC HYDROGENATION OF NITRILES TO PRODUCE CAPSAICINOID DERIVATIVES AND AMINE COMPOUNDS, AND METHODS FOR PURIFIYING AND OBTAINING THE POLYMORPHS THEREOF

Processes for preparing an amine compound by catalytically hydrogenating a precursor nitrile compound. In a particular aspect, the present hydrogenation process occurs in a dipolar organic solvent in the presence of a palladium/carbon catalyst and a strong anhydrous protic acid. In a further aspect, the preferred embodiment relates to a process for deprotecting a compound to produce an amine compound. In yet a further aspect, the preferred embodiment relates to amine products produced by the present processes. These amine products may be used for a variety of purposes.