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(4-METHOXY-BENZYL)-(2-METHOXY-1-METHYL-ETHYL)-AMINE is a tertiary amine compound characterized by the presence of a methoxybenzyl group and a methoxyethylamine group. Its structural arrangement, featuring aromatic and organic properties, suggests potential reactivity and applications in various chemical processes and industries. (4-METHOXY-BENZYL)-(2-METHOXY-1-METHYL-ETHYL)-AMINE's unique characteristics make it a valuable building block in organic synthesis and pharmaceutical research.

353777-78-3

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353777-78-3 Usage

Uses

Used in Pharmaceutical Research:
(4-METHOXY-BENZYL)-(2-METHOXY-1-METHYL-ETHYL)-AMINE is used as a building block for the development of new pharmaceutical compounds due to its unique structural arrangement and potential reactivity. The presence of methoxy and benzyl groups may contribute to the compound's interaction with biological targets, making it a promising candidate for drug discovery and design.
Used in Organic Synthesis:
In the field of organic synthesis, (4-METHOXY-BENZYL)-(2-METHOXY-1-METHYL-ETHYL)-AMINE is used as an intermediate for the synthesis of more complex organic molecules. Its structural features, including the methoxy and benzyl groups, can be exploited to create a variety of chemical products, such as agrochemicals, dyes, and other specialty chemicals.
Used in Chemical Process Industries:
(4-METHOXY-BENZYL)-(2-METHOXY-1-METHYL-ETHYL)-AMINE is utilized as a reagent or catalyst in various chemical processes, taking advantage of its tertiary amine nature and the presence of reactive functional groups. Its application in this industry can lead to the production of a wide range of chemical products with diverse applications.
Used in Material Science:
In the field of material science, (4-METHOXY-BENZYL)-(2-METHOXY-1-METHYL-ETHYL)-AMINE may be used as a component in the development of novel materials with specific properties, such as improved conductivity, enhanced stability, or unique optical characteristics. (4-METHOXY-BENZYL)-(2-METHOXY-1-METHYL-ETHYL)-AMINE's aromatic and organic properties make it a candidate for use in the creation of advanced materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 353777-78-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,7,7 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 353777-78:
(8*3)+(7*5)+(6*3)+(5*7)+(4*7)+(3*7)+(2*7)+(1*8)=183
183 % 10 = 3
So 353777-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H19NO2/c1-10(9-14-2)13-8-11-4-6-12(15-3)7-5-11/h4-7,10,13H,8-9H2,1-3H3

353777-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-N-[(4-methoxyphenyl)methyl]propan-2-amine

1.2 Other means of identification

Product number -
Other names (2-methoxy-isopropyl)[(4-methoxyphenyl)methyl]amine

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:353777-78-3 SDS

353777-78-3Upstream product

353777-78-3Downstream Products

353777-78-3Relevant academic research and scientific papers

Microwave-assisted regioselective ring opening of non-activated aziridines by lithium aluminium hydride

Stankovic, Sonja,D'Hooghe, Matthias,De Kimpe, Norbert

experimental part, p. 4266 - 4273 (2010/11/18)

A new synthetic protocol for the LiAlH4-promoted reduction of non-activated aziridines under microwave conditions was developed. Thus, ring opening of 2-(acetoxymethyl)aziridines provided the corresponding β-amino alcohols, which were then used as eligible substrates in the synthesis of 5-methylmorpholin-2-ones via condensation with glyoxal in THF. The same procedure was applied for the preparation of novel 5(R)- and 5(S)-methylmorpholin-2-ones starting from the corresponding enantiopure 2-(hydroxymethyl)aziridines. Additionally, 2-(methoxymethyl)- and 2-(phenoxymethyl)aziridines were treated with LiAlH4 under microwave irradiation, giving rise to either isopropylamines or 1-methoxypropan-2-amines depending on the reaction conditions.

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