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2,5-Dichloro-4-sulfo-benzenediazonium chloride is a chemical compound with the molecular formula C6H3Cl2N2O3S. It is a derivative of benzenediazonium, featuring two chlorine atoms at the 2nd and 5th positions, a sulfonate group at the 4th position, and a chloride counterion. 2,5-Dichloro-4-sulfo-benzenediazonium; chloride is typically used as an intermediate in the synthesis of various dyes and pigments, particularly those with high color strength and stability. Due to its reactive nature, it is important to handle 2,5-Dichloro-4-sulfo-benzenediazonium; chloride with care, following proper safety protocols to minimize potential hazards.

88-54-0

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88-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88-54-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88-54:
(4*8)+(3*8)+(2*5)+(1*4)=70
70 % 10 = 0
So 88-54-0 is a valid CAS Registry Number.

88-54-0Relevant academic research and scientific papers

The Influence of Chlorine and Sulphonate Substituents on the Visible Absorption Maxima of Some Azo Dyes

Greenwood, David,Hutchings, Michael G.,Lamble, Brian

, p. 1107 - 1114 (2007/10/02)

A total of 110 arylazo dyes have been prepared, based on five benzenoid and heterocyclic coupling components, and containing combinations of chlorine and sulphonate (sulpho) substituents in the diazo components.Their visible absorption maxima have been analysed in order to determine the degree to which chloro and sulfo substituent influences are constant and transferable, both within a series, and between series.Additivity is found to pertain, if allowances are made for steric effects.A 2-sulpho group alone can induce nonplanarity, depending on the nature of the coupling component.The 2-sulpho-3-chloro combination is particularly responsible for hypsochromic shifts unexpected on the basis of strict additivity.Computer-aided molecular modelling studies have clarified the steric interactions present.Di-ortho-substitution also induces nonplanarity and hypsochromic effects.There is some evidence for non-equivalence of a substituent in the two distinct meta-orientations, although MO calculations do not reproduce this behaviour.

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