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

96748-61-7

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96748-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96748-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,4 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96748-61:
(7*9)+(6*6)+(5*7)+(4*4)+(3*8)+(2*6)+(1*1)=187
187 % 10 = 7
So 96748-61-7 is a valid CAS Registry Number.

96748-61-7SDS

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-(cyclohexen-1-yl)ethenylbenzene

1.2 Other means of identification

Product number -
Other names 1-(1-cyclohexenyl)styrene

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:96748-61-7 SDS

96748-61-7Relevant academic research and scientific papers

Synthesis of Highly Substituted Polyenes by Palladium-Catalyzed Cross–Couplings of Sterically Encumbered Alkenyl Bromides and N-Tosylhydrazones

Paraja, Miguel,Barroso, Raquel,Cabal, M. Paz,Valdés, Carlos

supporting information, p. 1058 - 1062 (2017/03/27)

A new method for the synthesis of polysubstituted conjugated dienes is described, through the palladium-catalyzed cross-coupling between N-tosylhydrazones and alkenyl bromides. The reaction proceeds efficiently when a combination of a highly substituted bromoalkene and a hydrazone derived from a ketone are employed, pointing to the convenience of a sterically encumbered environment. This unprecedented process allows for the stereocontrolled preparation of highly substituted dienes and polyenes. (Figure presented.).

Selective arylation and vinylation at the α position of vinylarenes

Zou, Yinjun,Qin, Liena,Ren, Xinfeng,Lu, Yunpeng,Li, Yongxin,Zhou, Jianrong

supporting information, p. 3504 - 3511 (2013/07/05)

In intermolecular Heck reactions of styrene and vinylarenes, the aryl and vinyl groups routinely insert at the β position. However, selective insertion at the α position has been very rare. Herein, we provide a missing piece in the palette of Heck reaction, which gave >20:1 α selectivity. The key to our success is a new ferrocene 1,1′-bisphosphane (dnpf) that carries 1-naphthyl groups. Our mechanistic studies revealed that the high α selectivity is partly attributable to the steric effect of dnpf. The rigid and bulky 1-naphthyl groups of dnpf sterically disfavor β insertion. What the Heck! In intermolecular Heck reactions, insertion at the β position of aromatic olefins is very common, but reversal of the selectivity for selective α insertion has been a longstanding problem. A general method to couple aryl and vinyl triflates with aromatic olefins in >20:1 α selectivity is presented. The key to this successful approach is a new ferrocene bisphosphane with naphthyl groups on the phosphorus atom (see scheme; OTf=triflate). Copyright

Synthesis of 1,1-disubstituted olefins via catalytic alkyne hydrothiolation/Kumada cross-coupling

Sabarre, Anthony,Love, Jennifer

supporting information; experimental part, p. 3941 - 3944 (2009/06/18)

(Chemical Equation Presented) Using recently developed methodology for the regioselective formation of branched alkyl vinyl sulfides, we report a convenient route to 1,1-disubstituted olefins. We demonstrate that n-propanethiol successfully undergoes cata

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