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54478-82-9

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54478-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54478-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,7 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54478-82:
(7*5)+(6*4)+(5*4)+(4*7)+(3*8)+(2*8)+(1*2)=149
149 % 10 = 9
So 54478-82-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H5N2.H2O/c7-8-6-4-2-1-3-5-6;/h1-5H;1H2/q+1;/p-1

54478-82-9SDS

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 benzenediazonium,hydroxide

1.2 Other means of identification

Product number -
Other names Benzoldiazonium,Hydroxid

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:54478-82-9 SDS

54478-82-9Relevant articles and documents

Photooxidation of Arylazo-Naphtholes with Singlet Oxygen

Becker, H. G. O.,Franze, J.

, p. 957 - 964 (2007/10/02)

The reaction of p-substituted 4-arylazo-1-naphtholes 1 and 1-arylazo-2-naphtholes 5 with singlet oxygen (produced by methylene blue-sensitized photolysis) has been studied spectroscopically in methanol as a solvent.The rate constants of dye bleaching are the same, irrespective whether the extinctions of the azo or the hydrazone forms of the tautomeric systems are measured.Both reaction series 1 and 5 afford linear Hammett plots, which is discussed in the light of the azo-hydrazone equilibrium of the dyes and an "ene" mechanism of the reaction with singlet oxygen.It could be shown by short-time spectroscopy that the azo-hydrazone isomerization proceeds much faster than the attack of singlet oxygen on the hydrazone form, which explains all observed facts.

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