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Benzene, 1,4-bis[(1E)-2-(pentafluorophenyl)ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128207-26-1

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128207-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128207-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,0 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128207-26:
(8*1)+(7*2)+(6*8)+(5*2)+(4*0)+(3*7)+(2*2)+(1*6)=111
111 % 10 = 1
So 128207-26-1 is a valid CAS Registry Number.

128207-26-1SDS

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 1,2,3,4,5-pentafluoro-6-[2-[4-[2-(2,3,4,5,6-pentafluorophenyl)ethenyl]phenyl]ethenyl]benzene

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:128207-26-1 SDS

128207-26-1Relevant academic research and scientific papers

Fluorinated distyrylbenzene chromophores: effect of fluorine regiochemistry on molecular properties and solid-state organization

Renak, Michelle L.,Bartholomew, Glenn P.,Wang, Shujun,Ricatto, Pascal J.,Lachicotte, Rene J.,Bazan, Guillermo C.

, p. 7787 - 7799 (1999)

A series of fluorinated distyrylbenzene (DSB) derivatives were synthesized and studied in order to probe the effect of fluorine substitution on molecular properties and on the arrangement of molecules in the solid state. Reaction of 1,4-diiodobenzene with

Rh2(OAc)4-catalyzed formation of trans-alkenes from the reaction of aldehydes with perfluorophenyl diazomethane through tellurium ylide

Zhu, Shifa,Xing, Chunhui,Pang, Wan,Zhu, Shizheng

, p. 5897 - 5900 (2007/10/03)

Rh2(OAc)4 can catalyze the formation of perfluorophenyl-containing trans-epoxides from the reactions of perfluorophenyl diazomethane with activated aryl aldehydes through sulfur ylide intermediate. In contrast, under the same reactio

Transition-Metal-Catalyzed Formation of trans Alkenes via Coupling of Aldehydes

Zhu, Shifa,Liao, Yuanxi,Zhu, Shizheng

, p. 377 - 380 (2007/10/03)

(Equation presented) Rh2(OAc)4 catalyzed the formation of exclusively trans fluorinated alkenes from aldehydes and pentafluorobenzaldehyde tosylhydrazone salts, which were readily prepared from pentafluorobenzaldehyde using the Bamfo

Phenyl-perfluorophenyl stacking interactions: Topochemical [2+2] photodimerization and photopolymerization of olefinic compounds

Coates, Geoffrey W.,Dunn, Alex R.,Henling, Lawrence M.,Ziller, Joseph W.,Lobkovsky, Emil B.,Grubbs, Robert H.

, p. 3641 - 3649 (2007/10/03)

The face-to-face stacking interaction between phenyl and perfluorophenyl groups is emerging as a common noncovalent interaction. To explore the generality of this supramolecular synthon, the solid-state packing structure and reactivity of several monoolefins and diolefins substituted with phenyl and perfluorophenyl groups was investigated. Of the seven crystalline or cocrystalline materials investigated, six were found to undergo a photochemically induced [2+2] reaction in the solid state. By determining the stereochemistry of the photoproduct and/or X-ray structural analysis of the olefinic precursors, the stacked interaction between phenyl and perfluorophenyl groups in the photoactive crystals were revealed.

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