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Pyridinium, 1-[(3-chlorophenyl)methyl]-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59347-49-8

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59347-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59347-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,4 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59347-49:
(7*5)+(6*9)+(5*3)+(4*4)+(3*7)+(2*4)+(1*9)=158
158 % 10 = 8
So 59347-49-8 is a valid CAS Registry Number.

59347-49-8Relevant academic research and scientific papers

Conformational investigation of N-aralkylpyridinium ions by Cotton-Mouton effect method

Bulgarevich, S. B.,Bren, D. V.,Movshovic, D. Y.,Finocchiaro, P.,Failla, S.

, p. 147 - 156 (1994)

Molar Cotton-Mouton constants and refractions are reported at 298 K for the following N-aralkylpyridinium cations as solutes in water or acetonitrile: (C6H5)CH2(+NC5H5), (4-ClC6H4)CH2(+NC5H5), (3-ClC6H4)CH2(+NC5H5), (3-ClC

MUTUAL EFFECTS OF THE STRUCTURE IN THE REACTIONS OF BENZYL BROMIDES WITH PYRIDINES

Shpan'ko, I. V.,Korostylev, A. P.,Shved, E. N.,Litvinenko, L. M.

, p. 1562 - 1565 (2007/10/02)

The rate of the reactions of benzyl bromides with pyridines in nitrobenzene at 40 deg C was measured.The nonadditivity of the joint action of the electronic effects of substituents in the molecules of the reagents on the reactivity of the benzyl bromide-p

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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