Welcome to LookChem.com Sign In|Join Free
  • or
Pyridinium, 1-[(4-cyanophenyl)methyl]-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112503-30-7

Post Buying Request

112503-30-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

112503-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112503-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,0 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112503-30:
(8*1)+(7*1)+(6*2)+(5*5)+(4*0)+(3*3)+(2*3)+(1*0)=67
67 % 10 = 7
So 112503-30-7 is a valid CAS Registry Number.

112503-30-7Relevant academic research and scientific papers

Preparation method of [1-(4'-cyanobenzyl)pyridine][bis(maleonitriledithiolato)nickel (III)]

-

Paragraph 0037;0039-0040, (2018/10/11)

Belonging to the technical field of functional materials, the invention discloses a preparation method of an allomorph variant of [1-(4'-cyanobenzyl)pyridine][bis(maleonitriledithiolato)nickel (III)].The method utilizes I2 to oxidize [1-(4'-cyanobenzyl)pyridine]2[bis(maleonitriledithiolato)nickel (II)] to obtain [1-(4'-cyanobenzyl)pyridine][bis(maleonitriledithiolato)nickel (III)], then performing filtering at the end of the oxidation reaction, washing the filter cake N times, then dissolving the washed filter cake in acetonitrile, performing filtering, and volatilizing the filtrate for crystallization, thus obtaining the allomorph variant of bis(maleonitriledithiolato)nickel (III). The preparation method provided by the invention is simple and feasible, and the obtained product has highyield and high purity, and is suitable for industrial application.

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 112503-30-7