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1H-Imidazole, 2,5-dihydro-1-hydroxy-2,2,5,5-tetramethyl-4-(4-methylphenyl)-, 3-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84760-06-5

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84760-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84760-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,6 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84760-06:
(7*8)+(6*4)+(5*7)+(4*6)+(3*0)+(2*0)+(1*6)=145
145 % 10 = 5
So 84760-06-5 is a valid CAS Registry Number.

84760-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-4-tolyl-2,2,5,5-tetramethyl-3-imidazoline 3-oxide

1.2 Other means of identification

Product number -
Other names 2,2,5,5-Tetramethyl-3-oxy-4-p-tolyl-2,5-dihydro-imidazol-1-ol

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:84760-06-5 SDS

84760-06-5Upstream product

84760-06-5Relevant academic research and scientific papers

The Oxidative Properties of Nitroxy-radicals in Their Reactions with Sterically Hindered Hydroxylamines

Dikanov, S. A.,Grigor'ev, I. A.,Volodarskii, L. B.,Tsvetkov, Yu. D.

, p. 1696 - 1699 (2007/10/02)

A relative scale of the oxidative properties of cyclic nitroxy-radicals has been constructed and the influence of various structural factors on the oxidising capacity of the nitroxy-group in the radicals has been investigated.It is shown that the oxidative properties of the nitroxy-group in cyclic nitroxy-radicals become more pronounced with the increase in ring size.A relation has been established between the oxidative properties and the electron-accepting properties of functional groups separated from the nitroxy-group by two and more ?-bonds.

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