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Diazene, (4-methylphenyl)[phenyl(phenylhydrazono)methyl]-, (Z,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112080-45-2

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112080-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112080-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,8 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112080-45:
(8*1)+(7*1)+(6*2)+(5*0)+(4*8)+(3*0)+(2*4)+(1*5)=72
72 % 10 = 2
So 112080-45-2 is a valid CAS Registry Number.

112080-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(p-methylphenyl)-3,5-diphenylformazan

1.2 Other means of identification

Product number -
Other names 5-[4-Methyl-phenyl]-1,3-diphenyl-formazan

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:112080-45-2 SDS

112080-45-2Relevant academic research and scientific papers

Synthesis, spectroscopy, and quantum-chemical calculations on 1-substituted phenyl-3,5-diphenylformazans

Tezcan, Habibe,Tokay, Nesrin

, p. 54 - 60 (2010)

In this study 1-substituted phenyl-3,5-diphenylformazans were synthesized from benzaldehyde-N-phenylhydrazone and appropriate phenyldiazonium salts having CH3, Br, and Cl at the o-, m-, and p-positions of 1-phenyl ring. Their structures were determined by infrared and ultraviolet-visible spectra. Bathochromic effect in accordance with the electron-donating effect of CH3, Br, and Cl group and its magnitude were dependent upon type and position of substituent on the ring. The ground-state geometries and absorption wavelengths for 1-phenyl substituted formazans were studied with density functional theory and time-dependent density functional theory. The calculations were carried out by using PBE1PBE functional with 6-311G(2d,2p) basis set for λmax of the UV-vis spectra for the studied formazans. A good agreement was obtained between the experimental and computed values.

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