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125138-11-6

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125138-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125138-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,3 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 125138-11:
(8*1)+(7*2)+(6*5)+(5*1)+(4*3)+(3*8)+(2*1)+(1*1)=96
96 % 10 = 6
So 125138-11-6 is a valid CAS Registry Number.

125138-11-6SDS

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-(diethoxyphosphorylmethyl)-2,3,4,5,6-pentafluorobenzene

1.2 Other means of identification

Product number -
Other names diethyl (pentafluorobenzyl)phosphonate

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:125138-11-6 SDS

125138-11-6Relevant articles and documents

Supramolecular packing of alkyl substituted Janus face all-cis2,3,4,5,6-pentafluorocyclohexyl motifs

Clark, Joshua L.,Cordes, David B.,Cormanich, Rodrigo A.,Geddis, Ailsa,Guldin, Stefan,Neyyappadath, Rifahath M.,O'Hagan, David,Piscelli, Bruno A.,Slawin, Alexandra M. Z.,Taylor, Alaric,Yu, Cihang

, p. 9712 - 9719 (2021/07/28)

This study uses X-ray crystallography, theory and Langmuir isotherm analysis to explore the conformations and molecular packing of alkyl all-cis2,3,4,5,6-pentafluorocyclohexyl motifs, which are prepared by direct aryl hydrogenations from alkyl- or vinyl-pentafluoroaryl benzenes. Favoured conformations retain the more polar triaxial C-F bond arrangement of the all-cis2,3,4,5,6-pentafluorocyclohexyl ring systems with the alkyl substituent adopting an equatorial orientation, and accommodating strong supramolecular interactions between rings. Langmuir isotherm analysis on a water subphase of a long chain fatty acid and alcohol carrying terminal all-cis2,3,4,5,6-pentafluorocyclohexyl rings do not show any indication of monolayer assembly relative to their cyclohexane analogues, instead the molecules appear to aggregate and form higher molecular assemblies prior to compression. The study indicates the power and potential of this ring system as a motif for ordering supramolecular assembly.

A solution-based approach to composite dielectric films of surface functionalized CaCu3Ti4O12 and P(VDF-HFP)

Ehrhardt, Claudia,Fettkenhauer, Christian,Glenneberg, Jens,Muenchgesang, Wolfram,Leipner, Hartmut S.,Diestelhorst, Martin,Lemm, Sebastian,Beige, Horst,Ebbinghaus, Stefan G.

, p. 2266 - 2274 (2014/02/14)

High permittivity CaCu3Ti4O12/ poly(vinylidenefluoride-co-hexafluoropropylene) P(VDF-HFP) nanocomposites were investigated as dielectrics for film capacitors. CaCu3Ti 4O12 was synthesized by two different soft-chemistry methods, namely, decomposition of a citrate precursor and a recently developed lactate precursor to identify a preferable route to nanometer scale spherical particles with an increased interfacial area. A ball-milling step was applied to break particle agglomerates and to enhance particle distribution in the composite films. To improve the wetting of the CaCu3Ti 4O12 oxide particles and the polymer, a variety of surfactants, e.g. carbonic acid, silane, sulfonic acid and phosphonic acid were investigated. A successful oxide surface functionalization was achieved by 2,3,4,5,6-pentafluorobenzyl phosphonic acid, leading to stable bonds and good structural compatibility between the surfactant and the highly fluorinated polymer matrix. The films were prepared from composite dispersions by a spin-coating technique and can be formed out of powders from both precursors, but the citrate method is preferable due to milder synthesis conditions and improved film homogeneity. The use of ball-milled powders as the oxide component results in homogeneous particle distributions even near to the percolation threshold. In addition, such fine-ground particles lead to homogeneous film thickness and decreased film roughness. Dielectric measurements at different frequencies revealed an enhancement in the relative permittivity by a factor of 5 compared to the pure polymer while the dielectric losses remained very low.

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