501-06-4

Basic information

• Product Name: N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine
• Synonyms: Belladine;N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine
• CAS NO: 501-06-4
• Molecular Formula: C₁₉H₂₅NO₃
• Molecular Weight: 315.4067
• Mol File: 501-06-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 423.7°Cat760mmHg
• Flash Point: 119.3°C
• Appearance: /
• Density: 1.068g/cm³
• Vapor Pressure: 2.18E-07mmHg at 25°C
• Refractive Index: 1.544
• CAS DataBase Reference: N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine(501-06-4)
• EPA Substance Registry System: N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine(501-06-4)

Safety Data

• Hazardous Substances Data: 501-06-4(Hazardous Substances Data)

Usage

Definition

ChEBI: A phenethylamine alkaloid that is N-methyl-4-methoxyphenylethylamine carrying an additional N-(3,4-dimethoxybenzyl) substituent.

InChI:InChI=1/C19H25NO3/c1-20(12-11-15-5-8-17(21-2)9-6-15)14-16-7-10-18(22-3)19(13-16)23-4/h5-10,13H,11-12,14H2,1-4H3

Upstream product

• 121-33-5 vanillin 
• 51-67-2 tyrosamine 
• 88205-07-6 4-[2-(3,4-dimethoxy-benzylamino)ethyl]phenol 
• 74-88-4 methyl iodide 
• 50-00-0 formaldehyd 
• 40172-00-7 N-demethylbelladine 

Relevant articles and documents

A new lead compound for abscisic acid biosynthesis inhibitors targeting 9-cis-epoxycarotenoid dioxygenase

9-cis-Epoxycarotenoid dioxygenase (NCED), a key enzyme in abscisic acid (ABA) biosynthesis, cleaves the olefinic double bond of 9-cis-epoxycarotenoid. Several analogues of nordihydroguaiaretic acid (NDGA) were designed and synthesized, and their efficacy

ISOCRAUGSODINE, AN N-ARYLIDENEPHENETHYLAMINE FROM CRINUM ASIATICUM AND ITS E-Z ISOMERISM

A new Shiff's base, named isocraugsodine, was isolated from the fruits of Crinum asiaticum.Its N-(3-methoxy-4-hydroxybenzylidene)-4'-hydroxyphenethylamine structure was assigned on the basis of chemical transformation and comprehensive spectroscopic evidence.The temperature-gradient distribution of the three isomeric forms (1a1b1c) of the Shiff's base was determined by high resolution 1H NMR analysis.Isocraugsodine is considered as a direct precursor to Amaryllidaceae alkaloids.Key Word Index-Crinum asiaticum; Amaryllidaceae; N-(3-methoxy-4-hydroxybenzylidene)-4'-hydroxyphenethylamine; isocraugsodine; E-Z isomerism.