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N-(3-bromobenzyl)benzenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

251966-53-7

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251966-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251966-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,9,6 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 251966-53:
(8*2)+(7*5)+(6*1)+(5*9)+(4*6)+(3*6)+(2*5)+(1*3)=157
157 % 10 = 7
So 251966-53-7 is a valid CAS Registry Number.

251966-53-7Relevant academic research and scientific papers

USE OF COMPOSITIONS OBTAINED BY CALCINING PARTICULAR METAL-ACCUMULATING PLANTS FOR IMPLEMENTING CATALYTICAL REACTIONS

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Paragraph 0855, (2016/01/25)

The use of metal-accumulating plants for implementing chemical reactions especially catalytical reactions.

Inversion of the reactivity of benzyl bromides in reactions with anilines in dioxane and its mixtures with dimethyl sulfoxide. Experimental proof for isoparametric relationships

Shpan'ko

, p. 1010 - 1013 (2007/10/03)

Analysis of the structure-reactivity cross correlations shows the existence of isoparametric relationships in the reaction of Y-substituted benzyl bromides with X-substituted anilines in dioxane and 2, 3, and 5 M solutions of dimethyl sulfoxide in dioxane

EFFECTS OF SUBSTITUENTS IN THE BENZYL BROMIDE ON THE KINETICS OF THE BENZYLATION OF AMINES

Shpan'ko, I. V.,Korostylev, A. P.,Rusu, L. N.

, p. 1715 - 1723 (2007/10/02)

The kinetics of the reactions of 3- and 4-substituted benzyl bromides with amines having various structures in nitrobenzene at 40 deg C were investigated.The 4-substituted benzyl bromides have higher reactivity compared with that calculated on the basis of the linear correlations according to the Hammett-Taft equation for unsubstituted and 3-substituted benzyl bromides containing electron-withdrawning substituents.The reactivity of benzyl bromides containing electron-donating substituents obeys a linear correlation with the ?+ constants.The effects of structural changes in the substrate and the nucleophile on the character of the transition states of the investigated reactions is discussed.

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