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2H-Indole-3,7-dione, 2-methyl-2-phenyl-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65817-73-4

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65817-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65817-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,1 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65817-73:
(7*6)+(6*5)+(5*8)+(4*1)+(3*7)+(2*7)+(1*3)=154
154 % 10 = 4
So 65817-73-4 is a valid CAS Registry Number.

65817-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-oxy-2-phenyl-2H-indole-3,7-dione

1.2 Other means of identification

Product number -
Other names 2-methyl-3,7-dioxo-2-phenyl-3,7-dihydro-2H-indole 1-oxide

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:65817-73-4 SDS

65817-73-4Relevant academic research and scientific papers

On the Reaction of Aminoxyls with Dioxiranes

Dinoi, Anna,Curci, Ruggero,Carloni, Patricia,Damiani, Elisabetta,Stipa, Pierluigi,Greci, Lucedio

, p. 871 - 876 (2007/10/03)

In the reactions of dimethyldioxirane (1a) and methyl(trifluoromethyl)dioxirane (1b) with 2,2,6,6-tetramethylpiperidinyl-1-oxyl (2) (TEMPO) in acetone, the corresponding methoxyamine 1-methoxy-2,2,6,6-tetramethylpiperidine (5) is produced in ≥98% yield, b

HOMOLYTIC SUBSTITUTIONS IN INDOLINONE NITROXIDE RADICALS-III REACTIONS WITH TERBUTOXY AND METHYL RADICALS

Greci, L.

, p. 2435 - 2440 (2007/10/02)

Nitroxide radicals 1a-c react with terbutoxy radical to form terbutoxy substituted radicals 2, 3 and 4.The reaction mechanism is interpreted in terms of homolytic substitution.The terbutoxy substituted nitroxides can be easily oxidized to quinoneimine N-o

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