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56818-02-1

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56818-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56818-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,1 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56818-02:
(7*5)+(6*6)+(5*8)+(4*1)+(3*8)+(2*0)+(1*2)=141
141 % 10 = 1
So 56818-02-1 is a valid CAS Registry Number.

56818-02-1SDS

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 2,3,4,6-tetrachloro-phenetole

1.2 Other means of identification

Product number -
Other names 2.3.4.6-Tetrachlor-1-aethoxy-benzol

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:56818-02-1 SDS

56818-02-1Downstream Products

56818-02-1Relevant articles and documents

Polyhalogenoaromatic Compounds. Part 46. Circumstantial Evidence for the Intermediacy of Radical Anions during the Reaction of Magnesium with ω-Bromoalkoxypolychloro-arenes and -heteroarenes

Wakefield, Basil J.,Whitten, Jeffrey P.,Farley, Paul S.

, p. 93 - 100 (2007/10/02)

4-(ω-Bromoalkoxy)tetrachloropyridines, 4-(ω-bromoalkoxy)-3,5-dichloro-2,6-difluoropyridines, and (ω-bromoalkoxy)-pentachlorobenzenes have been prepared by reaction of the appropriate aryl and heteroaryl oxides with 1,ω-dibromoalkanes.The main products from the reactions of the bromoethoxy- or bromopropoxy-tetrachloropyridines with magnesium were the furopyridine (9a) and pyranopyridine (9b), respectively.Elimination of other possible reaction pathways leads to the hypothesis that the cyclisations proceed by electron transfer from magnesium to the tetrachloropyridyl group, followed by nucleophilic displacement of bromide from the side chain.In the absence of a leaving group in the side chain, the radical-anion intermediate leads to a Grignard reagent.

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