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89039-18-9

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89039-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89039-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,3 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89039-18:
(7*8)+(6*9)+(5*0)+(4*3)+(3*9)+(2*1)+(1*8)=159
159 % 10 = 9
So 89039-18-9 is a valid CAS Registry Number.

89039-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-chloro-2-(4-methylphenyl)ethyl]sulfanyl-2,4-dinitrobenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-[[2-chloro-2-(4-methylphenyl)ethyl]thio]-2,4-dinitro

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:89039-18-9 SDS

89039-18-9Downstream Products

89039-18-9Relevant articles and documents

Carbon-14 Kinetic Isotope Effects and Mechanisms of Addition of 2,4-Dinitrobenzenesulfenyl Chloride to Substituted Styrenes-1-14C and Styrenes-2-14C

Kanska, Marianna,Fry, Arthur

, p. 7666 - 7672 (1983)

As the first reported examples of carbon isotope effects in simple electrophilic addition reactions we have measured the carbon-14 kinetic isotope effects in the addition of 2,4-dinitrobenzenesulfenyl chloride to a series of para-substituted α- and β-labe

COMPETING DIRECTIONS IN THE REACTIONS OF COMPOUNDS OF ELECTROPHILIC SULFUR WITH ALKENES

Bodrikov, I. V.,Ganzhenko, T. S.,Sokova, F. M.,Zefirov, N. S.

, p. 217 - 226 (2007/10/02)

The products and the kinetic relationships of the reactions of chlorothiocyanogen, dithiocyanogen, and 2,4-dinitrobenzenesulfenyl halides with allylbenzenes and styrenes in acetic acid were investigated in the presence of lithium perchlorate and without additions.Considerable variation was found in the electrophilicity of the sulfur-containing reagents (the formation of only products from normal addition and/or solvated adducts and the products from skeletal rearrangement).The nature of the reagent has an effect on the degree of the effect of strong electrolytes in the control of the competing reactions.The kinetic relationships governing the reactions were investigated, and an analysis was made of the data from the reactions of sulfenyl halides with styrenes.

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