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189350-81-0

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189350-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189350-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,3,5 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 189350-81:
(8*1)+(7*8)+(6*9)+(5*3)+(4*5)+(3*0)+(2*8)+(1*1)=170
170 % 10 = 0
So 189350-81-0 is a valid CAS Registry Number.

189350-81-0SDS

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 (E)-2-(2'-chloroethenyl)pyridine

1.2 Other means of identification

Product number -
Other names (E)-2-(2-Chlorovinyl)pyridine

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:189350-81-0 SDS

189350-81-0Downstream Products

189350-81-0Relevant articles and documents

Partial Reduction and Selective Transfer of Hydrogen Chloride on Catalytic Gold Nanoparticles

Oliver-Meseguer, Judit,Doménech-Carbó, Antonio,Boronat, Mercedes,Leyva-Pérez, Antonio,Corma, Avelino

supporting information, p. 6435 - 6439 (2017/05/29)

HCl in solution accepts electron density from Au NPs and partially reduces at room temperature, as occurs with other simple diatomic molecules, such as O2 and H2. The activation can be run catalytically in the presence of alkynes to give exclusively E-vinyl chlorides, after the regio- and stereoselective transfer of HCl. Based also on this method, vinyl chloride monomer (VCM) can be produced in a milder and greener way than current industrial processes.

Synthesis of 1,4-di(n-pyridyl)buta-1,3-diyne and formation of charge-transfer complexes. X-Ray structure of 1,4-di(3-pyridyl)buta-1,3-diyne

Rodriguez, J. Gonzalo,Martin-Villamil, Rosa,Cano, Felix H.,Fonseca, Isabel

, p. 709 - 714 (2007/10/03)

Ethynylpyridines have been satisfactorily prepared by two different routes: (a) the Wittig reaction between chloromethylene(triphenyl)phosphine ylide and a pyridinecarbaldehyde, followed by elimination of hydrogen chloride; (b) from the 2-methyl-4-(n-pyridyl)but-3-yn-2-ol intermediate, by elimination of acetone. 1,4-Di(n-pyridyl)buta-1,3-diynes are obtained by oxidative dimerization in good yield. An X-ray structure of the 3-substituted dimer is reported. Mono- and di-methyl salts of the 3-substituted diyne have been obtained and the charge-transfer complexes with tetramethyl-p-phenylenediamine (TMPD) are formed.

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