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31032-94-7

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31032-94-7 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 48, p. 903, 1983 DOI: 10.1021/jo00154a038

Check Digit Verification of cas no

The CAS Registry Mumber 31032-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,3 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31032-94:
(7*3)+(6*1)+(5*0)+(4*3)+(3*2)+(2*9)+(1*4)=67
67 % 10 = 7
So 31032-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H14/c1-3-11-9-13-7-5-4-6-12(13)8-10(11)2/h4-9H,3H2,1-2H3

31032-94-7SDS

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-ethyl-3-methylnaphthalene

1.2 Other means of identification

Product number -
Other names 2-Ethyl-3-methylnaphthalene

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:31032-94-7 SDS

31032-94-7Downstream Products

31032-94-7Relevant articles and documents

The Anion from 2,3-Dimethylnaphthalene/Tetramethylethylenediamine/n-Butyllithium: An Unusual Ambident Aromatic Nucleophile

Mitchell, Reginald H.,Dingle, Thomas W.,Williams, Richard Vaughan

, p. 903 - 905 (1983)

-

Lewis acid catalyzed inverse electron-demand diels-alder reaction of 1,2-diazines

Kessler, Simon N.,Wegner, Hermann A.

supporting information; experimental part, p. 4062 - 4065 (2010/11/17)

A systematic approach toward Lewis acid catalyzed inverse electron-demand Diels-Alder (IEDDA) reactions of 1,2-diazines is described. The general concept is first investigated by DFT calculations, supported by spectroscopic data, and finally proven in the experiment.

Intramolecular Reaction Of Nitroxide Radicals With Biradical Intermediates Generated From Aromatic Enediynes

Grissom, Janet Wisniewski,Gunawardena, Gamini U.

, p. 4951 - 4954 (2007/10/02)

1,4-Dehydronaphthalene biradicals generated by thermolysis of aromatic enediynes can be trapped with the nitroxide radical TEMPO.The isolated products, however, are not the direct trapping products but 1,4-naphthoquinones resulting from the homolysis of N-O bonds of trapping products.

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