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543731-16-4

Benzenemethanamine, N,4-dimethoxy(9CI), also known as 4-methoxyphenethylamine, is a chemical compound with the molecular formula C9H13NO2. It belongs to the class of organic compounds known as anisoles and is a derivative of phenethylamine. Benzenemethanamine, N,4-dimethoxy(9CI) features a benzene ring with two methoxy groups attached to the fourth carbon atom. Benzenemethanamine, N,4-dimethoxy(9CI) is commonly used in pharmaceutical research and has potential therapeutic applications due to its impact on the central nervous system. It is important to handle this chemical with care, as it can be hazardous if not used properly.

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  • 543731-16-4 Structure

  • Basic information

    1. Product Name: Benzenemethanamine, N,4-dimethoxy- (9CI)
    2. Synonyms: N-(4-Methoxybenzyl)-O-MethylhydroxylaMine;Benzenemethanamine, N,4-dimethoxy- (9CI)
    3. CAS NO:543731-16-4
    4. Molecular Formula: C9H13NO2
    5. Molecular Weight: 167.20502
    6. EINECS: N/A
    7. Product Categories: METHOXY
    8. Mol File: 543731-16-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzenemethanamine, N,4-dimethoxy- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanamine, N,4-dimethoxy- (9CI)(543731-16-4)
    11. EPA Substance Registry System: Benzenemethanamine, N,4-dimethoxy- (9CI)(543731-16-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 543731-16-4(Hazardous Substances Data)

543731-16-4 Usage

Uses

Used in Pharmaceutical Research:
Benzenemethanamine, N,4-dimethoxy(9CI) is used as a research compound for studying its potential therapeutic applications. Its impact on the central nervous system makes it a valuable candidate for further investigation in the development of new medications.
Used in Drug Development:
Due to its effects on the central nervous system, Benzenemethanamine, N,4-dimethoxy(9CI) is used as a starting material or intermediate in the synthesis of various pharmaceuticals. This allows researchers to explore its potential in treating a range of conditions and disorders.
Used in Chemical Synthesis:
Benzenemethanamine, N,4-dimethoxy(9CI) is also used as a building block in the synthesis of other organic compounds. Its unique structure and functional groups make it a versatile component in the creation of new molecules with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 543731-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,3,7,3 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 543731-16:
(8*5)+(7*4)+(6*3)+(5*7)+(4*3)+(3*1)+(2*1)+(1*6)=144
144 % 10 = 4
So 543731-16-4 is a valid CAS Registry Number.

543731-16-4SDS

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 N-methoxy-1-(4-methoxyphenyl)methanamine

1.2 Other means of identification

Product number -
Other names N-4-Methoxybenzyl-O-methyl-hydroxylamine

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:543731-16-4 SDS

543731-16-4Downstream Products

543731-16-4Relevant articles and documents

HYDROGENATION PROCESS OF OXIME DERIVATIVES

-

Page/Page column 27; 29, (2020/06/01)

The present invention relates to a novel process for the iridium-catalysed hydrogenation of oximes. The invention also relates to novel iridium catalysts for use in the iridium-catalysed hydrogenation of oximes and to processes of preparation of these cat

One-pot synthesis of alkoxyamine derivatives by reductive alkoxyamination with a 2-picoline-borane complex

Kawase, Yasushi,Yamagishi, Takehiro,Kutsuma, Teruo,Ueda, Kimio,Iwakuma, Takeo,Nakata, Tadashi,Yokomatsu, Tsutomu

experimental part, p. 463 - 470 (2009/06/08)

Reduction of oxime ethers with a 2-picoline-borane complex was examined to give alkoxyamine derivatives. The reduction was found to proceed in the presence of aqueous HCl in MeOH-AcOH. The method was extended to one-pot synthesis of alkoxyamine derivative

Intramolecular catalytic Friedel-Crafts reactions with allenyl cations for the synthesis of quinolines and their analogues

Ishikawa, Teruhiko,Manabe, Shinobu,Aikawa, Toshiaki,Kudo, Takayuki,Saito, Seiki

, p. 2361 - 2364 (2007/10/03)

(Equation Presented) This paper describes a novel method to synthesize a quinoline backbone by incorporating allenyl cations into a catalytic intramolecular Friedel-Crafts reaction. The initial products were isomerized and aromatized upon treatment with acid and base, respectively, to give quinolines. The basic concept also proved to be promising for 1-benzazepine, 1-benzazocine, or isoquinoline synthesis.

HIV Integrase inhibitors

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, (2008/06/13)

The present invention relates to the inhibition of HIV integrase, and to the treatment of AIDS or ARC by administering compounds of the following formula, or a tautomer of said compound, or a pharmaceutically acceptable salt, solvate or prodrug thereof: wherein R1, R2 and B1 are as defined herein.

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