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26620-11-1

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26620-11-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26620-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,2 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26620-11:
(7*2)+(6*6)+(5*6)+(4*2)+(3*0)+(2*1)+(1*1)=91
91 % 10 = 1
So 26620-11-1 is a valid CAS Registry Number.

26620-11-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethenylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names trans-1-chloro-2-phenylsulfanyl-ethylene

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:26620-11-1 SDS

26620-11-1Relevant articles and documents

Novel stereoselective phase transfer catalytic synthesis and some applications of (E)-2-chlorovinylthioarenes and hetarenes

Rubina, Kira,Abele, Edgars,Popelis, Juris,Grinberga, Solveiga,Arsenyan, Pavel,Lukevics, Edmunds

, p. 521 - 529 (2007/10/03)

A novel two-step method for the preparation of (E)-2-chlorovinyl-thioarenes (or hetarenes) from thiols and 1,1,2-trichloroethane in the phase transfer catalytic systems solid K2CO3/solid KI/18-crown-6/xylene and solid KOH/18-crown-6/

HIGH-TEMPERATURE ORGANIC SYNTHESIS. XXXIX. GAS-PHASE REACTION OF THIOPHENOL WITH 1,2-DICHLOROETHENE

Ivanova, N. D.,Korchevin, N. A.,Sigalov, M. V.,Keiko, V. V.,Deryagina, E. N.,Voronkov, M. G.

, p. 572 - 575 (2007/10/02)

Thiophenol reacts with 1,2-dichloroethene (a 3:1 mixture of E and Z isomers) in the gas phase at 400-550 deg C forming phenyl β-chlorovinyl sulfide (E and Z isomers, 1:1) with an overall yield of up to 84percent.The products from its further thermal transformations are benzothiophene. 3-chlorobenzothiophene, 1,2-bis(phenylthio)ethene (a mixture of stereoisomers), and 3-phenylthiobenzothiophene

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