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Benzene, 1-ethenyl-2-(2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21919-44-8

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21919-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21919-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,1 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21919-44:
(7*2)+(6*1)+(5*9)+(4*1)+(3*9)+(2*4)+(1*4)=108
108 % 10 = 8
So 21919-44-8 is a valid CAS Registry Number.

21919-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenyl-2-prop-2-enylbenzene

1.2 Other means of identification

Product number -
Other names o-allylstyrene

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:21919-44-8 SDS

21919-44-8Relevant academic research and scientific papers

2,2,3,3-tetrafluoronickelacyclopentanes generated via the oxidative cyclization of tetrafluoroethylene and simple alkenes: A key intermediate in nickel-catalyzed C-C bond-forming reactions

Ohashi, Masato,Kawashima, Takuya,Taniguchi, Tomoaki,Kikushima, Kotaro,Ogoshi, Sensuke

supporting information, p. 1604 - 1607 (2015/05/20)

Oxidative cyclization of tetrafluoroethylene (TFE) and ethylene with Ni(0) resulted in the formation of a five-membered nickelacycle. In the presence of PPh3 as an auxiliary ligand, the partially fluorinated five-membered nickelacycle was isolated and the structure was determined by X-ray analysis. This nickelacycle was found not only to react stoichiometrically with enones to give a cross-trimerization product but also to be a key reaction intermediate in the Ni(0)-catalyzed cotrimerization of TFE and ethylene, leading to 5,5,6,6-tetrafluoro-1-hexene.

Expanding the regioselective enzymatic repertoire: Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta

Paul, Caroline E.,Rajagopalan, Aashrita,Lavandera, Ivan,Gotor-Fernandez, Vicente,Kroutil, Wolfgang,Gotor, Vicente

supporting information; experimental part, p. 3303 - 3305 (2012/04/23)

The first report of a biocatalytic regioselective oxidative mono-cleavage of dialkenes was successfully achieved employing a cell-free enzyme preparation from Trametes hirsuta at the expense of molecular oxygen. Selected reactions were performed on a preparative scale affording high to excellent conversions and chemoselectivities. The Royal Society of Chemistry 2012.

Selective functionalization of arenes through the reaction of aryne-zirconocene complexes and enol ethers

Barluenga, José,Fernández, Amadeo,álvarez-Rodrigo, Lucía,Rodríguez, Félix,Fa?anás, Francisco J.

, p. 2513 - 2515 (2007/10/03)

A new method for the selective functionalization of aromatic rings by the zirconium promoted cross coupling reaction of an aryllithium compound and an enol ether is reported. Formation of an aryne-zirconocene complex and its regioselective coupling with a

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