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1142-18-3

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1142-18-3 Usage

Description

4-Benzyloxy-N-methylaniline 97% is a chemical compound characterized by its benzene and amine functional groups, typically used in scientific research and organic synthesis. It usually appears as an off-white to beige crystalline powder with a 97% purity level, indicating a high concentration of the active compound. The benzyl group provides stability to the molecule, while the methylaniline portion contributes to its chemical reactivity, suggesting its application potential in various chemical reactions. Appropriate safety measures must be taken while handling and storing due to possible chemical hazards.

Uses

Used in Scientific Research:
4-Benzyloxy-N-methylaniline 97% is used as a key component in scientific research for its properties and potential applications in various chemical reactions.
Used in Organic Synthesis:
In the field of organic synthesis, 4-Benzyloxy-N-methylaniline 97% is used as a building block for the synthesis of more complex organic compounds, taking advantage of its chemical reactivity and stability provided by the benzyl group.
Used in Chemical Reactions:
4-Benzyloxy-N-methylaniline 97% is used as a reactant in various chemical reactions, where its benzene and amine functional groups contribute to the formation of desired products.

Check Digit Verification of cas no

The CAS Registry Mumber 1142-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1142-18:
(6*1)+(5*1)+(4*4)+(3*2)+(2*1)+(1*8)=43
43 % 10 = 3
So 1142-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO/c1-15-13-7-9-14(10-8-13)16-11-12-5-3-2-4-6-12/h2-10,15H,11H2,1H3

1142-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-4-phenylmethoxyaniline

1.2 Other means of identification

Product number -
Other names 4-Benzyloxy-methylanilin

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:1142-18-3 SDS

1142-18-3Relevant articles and documents

Highly selective hydrogenation of amides catalysed by a molybdenum pincer complex: Scope and mechanism

Leischner, Thomas,Artús Suarez, Lluis,Spannenberg, Anke,Junge, Kathrin,Nova, Ainara,Beller, Matthias

, p. 10566 - 10576 (2019/12/02)

A series of molybdenum pincer complexes has been shown for the first time to be active in the catalytic hydrogenation of amides. Among the tested catalysts, Mo-1a proved to be particularly well suited for the selective C-N hydrogenolysis of N-methylated formanilides. Notably, high chemoselectivity was observed in the presence of certain reducible groups including even other amides. The general catalytic performance as well as selectivity issues could be rationalized taking an anionic Mo(0) as the active species. The interplay between the amide CO reduction and the catalyst poisoning by primary amides accounts for the selective hydrogenation of N-methylated formanilides. The catalyst resting state was found to be a Mo-alkoxo complex formed by reaction with the alcohol product. This species plays two opposed roles-it facilitates the protolytic cleavage of the C-N bond but it encumbers the activation of hydrogen.

Additions of azomethine ylides to fullerene C60 assisted by a removable anchor

Da Ros, Tatiana,Prato, Maurizio,Lucchini, Vittorio

, p. 4289 - 4297 (2007/10/03)

The addition of nitrile oxides to [60]fullerene, leading to isoxazolinofullerenes, can be reversed using reducing agents such as Mo(CO)6 or DIBALH. Thus, this reaction can be used; in principle, for protection/deprotection of [60]fullerene or f

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