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105547-61-3

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105547-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105547-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,4 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105547-61:
(8*1)+(7*0)+(6*5)+(5*5)+(4*4)+(3*7)+(2*6)+(1*1)=113
113 % 10 = 3
So 105547-61-3 is a valid CAS Registry Number.

105547-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5-Amino-3-methyl-1-phenyl-1H-pyrazol-4-ylazo)-4-chloro-benzenesulfonic acid

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:105547-61-3 SDS

105547-61-3Downstream Products

105547-61-3Relevant articles and documents

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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