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N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine is a phenethylamine alkaloid that features a unique molecular structure with an N-methyl-4-methoxyphenylethylamine backbone and an additional N-(3,4-dimethoxybenzyl) substituent. N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine is characterized by its complex arrangement of methoxy groups and a benzyl moiety, which may contribute to its potential biological activities and applications.

501-06-4

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501-06-4 Usage

Uses

Used in Pharmaceutical Industry:
N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine is used as a pharmaceutical compound for its potential therapeutic effects. Given its phenethylamine alkaloid nature, it may possess bioactive properties that can be harnessed for the development of new drugs, particularly in the areas of neurochemistry and psychopharmacology.
Used in Research Applications:
In the field of scientific research, N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine serves as a valuable research tool for studying the structure-activity relationships of phenethylamines and their derivatives. Its unique molecular features make it an interesting subject for investigations into the mechanisms of action, receptor interactions, and potential therapeutic applications.
Used in Chemical Synthesis:
N-[(3,4-Dimethoxyphenyl)methyl]-4-methoxy-N-methylbenzeneethanamine can be utilized as a starting material or intermediate in the synthesis of more complex organic compounds, including other phenethylamines and related alkaloids. Its presence in the synthesis process may lead to the creation of novel compounds with unique properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 501-06-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 501-06:
(5*5)+(4*0)+(3*1)+(2*0)+(1*6)=34
34 % 10 = 4
So 501-06-4 is a valid CAS Registry Number.
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

501-06-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name belladine

1.2 Other means of identification

Product number -
Other names N-[(3,4-dimethoxyphenyl)methyl]-2-(4-methoxyphenyl)-N-methylethanamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:501-06-4 SDS

501-06-4Downstream Products

501-06-4Relevant academic research and scientific papers

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

Han, Sun-Young,Kitahata, Nobutaka,Saito, Tamio,Kobayashi, Masatomo,Shinozaki, Kazuo,Yoshida, Shigeo,Asami, Tadao

, p. 3033 - 3036 (2007/10/03)

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

ABSCISIC ACID BIOSYNTHESIS INHIBITOR

-

Page 6, (2010/02/07)

Compounds represented by the following general formula (I) or salts thereof: wherein R1 represents hydrogen atom, hydroxyl group, or an alkoxy group; R2 represents hydroxyl group or an alkoxy group which may be substituted; R3/

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

Ghosal, Shibnath,Shanthy, Amirthalingam,Singh, Sushil K.

, p. 1849 - 1852 (2007/10/02)

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.

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