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4453-80-9

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4453-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4453-80-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,5 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4453-80:
(6*4)+(5*4)+(4*5)+(3*3)+(2*8)+(1*0)=89
89 % 10 = 9
So 4453-80-9 is a valid CAS Registry Number.

4453-80-9SDS

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 1,5-diphenyl-3-nitroformazan

1.2 Other means of identification

Product number -
Other names 3-nitro-1,5-diphenylformazan

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:4453-80-9 SDS

4453-80-9Relevant articles and documents

Synthesis and kinetics of electronically altered photochromic dithizonatophenylmercury(II) complexes

Von Eschwege, Karel G.

, p. 159 - 166 (2013/03/13)

A series of phenyl-substituted dithizones were synthesized, and preparation of the corresponding series of photochromic phenylmercury(II) complexes is for the first time reported. Adaption of previous methods enhanced synthesis convenience and product yields. A single crystal X-ray data collection of the ortho-S-methyl nitroformazan reaction intermediate was done. ADF computed molecular orbitals of the title compound show the HOMO and LUMO orbitals stretching along the entire ligand. The spontaneous back reaction kinetics of dithizonatophenylmercury(II) was studied at varied concentrations, temperatures and in different solvents. An exponential correlation was found between the rate of reverse isomerization and temperature, while increased solvent polarity and decreased molar mass facilitate higher return rates. The kinetic study of the series of twelve electronically altered complexes yielded a lowest rate of 0.0002 s-1 for the ortho-methyl derivative, while the highest rate of 0.0106 s-1 was measured for the meta-methoxy derivative.

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