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Diazenecarbonitrile, (4-fluorophenyl)-, (E)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79896-01-8

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79896-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79896-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79896-01:
(7*7)+(6*9)+(5*8)+(4*9)+(3*6)+(2*0)+(1*1)=198
198 % 10 = 8
So 79896-01-8 is a valid CAS Registry Number.

79896-01-8SDS

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 4-fluorobenzenediazocyanide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79896-01-8 SDS

79896-01-8Relevant academic research and scientific papers

Catalytic Sandmeyer cyanation as a synthetic pathway to aryl nitriles

Beletskaya, Irina P.,Sigeev, Alexander S.,Peregudov, Alexander S.,Petrovskii, Pavel V.

, p. 3810 - 3812 (2007/10/03)

The catalytic version of Sandmeyer reaction for a number of aryl diazonium salts was investigated. Aryl nitriles ArCN were obtained by the Cu(I)/Cu(II) catalyzed reactions of aryl diazonium salts with KCN in good yields. The reactions with diazonium salts with electron-withdrawing groups led to formation of a corresponding nitrile in a high yield. The yield was found to be lower for the compounds containing electron-donating groups.

UV AND IR SPECTRA OF SOME ARENEDIAZOCYANIDES AND THEIR RADICAL-ANIONS

Kachkurova, I. Ya.,Ashkinadze, L. D.,Shamsutdinova, M. Kh.,Kazitsyna, L. A.

, p. 1629 - 1634 (2007/10/02)

The UV and IR spectra of some arenediazocyanides and their radical-anions with the general formula p-X-C6H4N=NCN, where X=CH3O, CN, NO2, CNN=N, CNC6H4, NO2C6H4, CNN=NC6H4, NO2C6H4S, CNN=NC6H4O, CNN=NC6H4S, were studied.During radical formation long-wave absorption bands appear in the UV spectrum in the region of 600-700 nm.The frequencies of the absorption band for the nitrile group (Δν 80-95 cm-1) in the IR spectrum are shifted substantially.The integral intensities ACN increase by two orders of magnitude.The obtained experimental data show that during radical formation from the arenediazocyanides the additional electron is concentrated mainly at the diazocyanide group, and in the binuclear systems the effect of the anionic substituent N=NCN(1-) is not transmitted to the second benzene ring.It is suggested that the special features in the spectral characteristics of the arenediazocyanides and their radical-anions are due to the specific structural character of the azo group.

Phase-Transfer Synthesis of Arenediazocyanides and Synthesis of Arenediazosulfones from Arenediazonium Cations and the Formation of Reduced Pyridazines by 2 + 4 Cycloaddition Reactions

Ahern, Michael F.,Leopold, Ahuva,Beadle, James R.,Gokel, George W.

, p. 548 - 554 (2007/10/02)

The remarkably versatile arenediazonium cations are also convenient to use and nondangerous when utilized as the BF4 or PF6 salts.Arenediazonium compounds have recently been shown to undergo the 2 + 4 Diels-Alder cycloaddition, but the reaction is solvent

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