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Benzene, [2-(1-cyclobuten-1-yl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57822-29-4

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57822-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57822-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,2 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57822-29:
(7*5)+(6*7)+(5*8)+(4*2)+(3*2)+(2*2)+(1*9)=144
144 % 10 = 4
So 57822-29-4 is a valid CAS Registry Number.

57822-29-4SDS

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-(cyclobuten-1-yl)ethylbenzene

1.2 Other means of identification

Product number -
Other names -

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:57822-29-4 SDS

57822-29-4Downstream Products

57822-29-4Relevant academic research and scientific papers

PtCl2-catalyzed rearrangement of methylenecyclopropanes

Fuerstner, Alois,Aissa, Christophe

, p. 6306 - 6307 (2007/10/03)

Alkylidenecyclopropanes readily convert into cyclobutene derivatives on treatment with catalytic amounts of PtCl2. The reaction is strongly accelerated when performed under an atmosphere of CO (1 atm). The resulting cyclobutenes are isolated in

Zirconium-Mediated Cross-Coupling of Terminal Alkynes and Vinyl Bromides: Selective Synthesis of Cyclobutene and 1,3-Diene Derivatives

Barluenga, Jose,Rodriguez, Felix,Alvarez-Rodrigo, Lucia,Fananas, Francisco J.

, p. 101 - 108 (2007/10/03)

A diastereoselective synthesis of 1,3-butadiene or cyclobutene derivatives by a zirconium-mediated reaction of alkenyllithium compounds and vinyl bromides is reported. The key steps involve the generation of zirconocene-alkyne complexes from haloalkenes and subsequent coupling with alkenyl bromides. Thus, formally the process supposes the cross-coupling reaction between a terminal alkyne and an alkenyl bromide. Moreover, the use of butyl vinyl ether instead of vinyl bromide as the unsaturated system allows an alternative access to different 1,3-butadiene regioisomers.

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