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Benzenemethanamine, N-(4-methoxyphenyl)-4-methyl-N-(phenylmethyl)-, also known as 4-(4-methoxyphenyl)-N-methyl-N-(phenylmethyl)aniline or 4-methoxy-alpha-methyldiphenylmethylamine, is an organic compound with the chemical formula C18H21NO. It is a derivative of benzenemethanamine, featuring a 4-methoxyphenyl group, a 4-methyl group, and a phenylmethyl group attached to the nitrogen atom. Benzenemethanamine, N-(4-methoxyphenyl)-4-methyl-N-(phenylmethyl)- is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also known for its potential applications in the development of new materials and as a research tool in the field of organic chemistry.

62849-46-1

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62849-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62849-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,4 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62849-46:
(7*6)+(6*2)+(5*8)+(4*4)+(3*9)+(2*4)+(1*6)=151
151 % 10 = 1
So 62849-46-1 is a valid CAS Registry Number.

62849-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-4-methoxy-N-(4-methylbenzyl)aniline

1.2 Other means of identification

Product number -
Other names -

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

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More Details:62849-46-1 SDS

62849-46-1Downstream Products

62849-46-1Relevant academic research and scientific papers

“One pot” synthesis of tertiary amines: Ru(II) catalyzed direct reductive N-benzylation of imines with benzyl bromide derivatives

Li, Bin,Yu, Jinghao,Li, Caihua,Li, Yibiao,Luo, Jianli,Shao, Yan

supporting information, p. 137 - 141 (2016/12/26)

The direct reductive N-benzylation of imines by reaction with benzyl bromide derivatives, in the presence of [RuCl2(p-cymene)]2catalyst and PhSiH3, is performed under mild conditions without additional base. This reaction proceeds by a tandem imine hydrosilylation/nucleophilic substitution with benzyl bromide derivatives to result the tertiary amines.

Copper-catalyzed N- and O-alkylation of amines and phenols using alkylborane reagents

Sueki, Shunsuke,Kuninobu, Yoichiro

supporting information, p. 1544 - 1547 (2013/06/26)

By the reaction of amines with alkylborane reagents in the presence of a catalytic amount of copper(II) acetate Cu(OAc)2 and di-tert-butyl peroxide, a cross-coupling reaction proceeded and alkylated amines were obtained in good to excellent yields. Phenols are also applicable for this reaction, and the corresponding alkyl aryl ethers were produced.

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