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Silane, chlorodimethyl(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65118-86-7

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65118-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65118-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,1 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65118-86:
(7*6)+(6*5)+(5*1)+(4*1)+(3*8)+(2*8)+(1*6)=127
127 % 10 = 7
So 65118-86-7 is a valid CAS Registry Number.

65118-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-dimethyl-(1-phenylethyl)silane

1.2 Other means of identification

Product number -
Other names Silane,chlorodimethyl(1-phenylethyl)

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:65118-86-7 SDS

65118-86-7Relevant academic research and scientific papers

Waste-free and efficient hydrosilylation of olefins

Pandarus, Valerica,Ciriminna, Rosaria,Gingras, Geneviève,Béland, Fran?ois,Kaliaguine, Serge,Pagliaro, Mario

, p. 129 - 140 (2019/01/11)

High purity silicone precursors can now be synthesized by hydrosilylation of solvent-free olefins catalyzed by a highly stable and active glass hybrid catalyst consisting of mesoporous organosilica microspheres doped with Pt nanoparticles. These findings open the door to the sustainable manufacture of silicone and a way to further reduce the amount of platinum in silicones, which are ubiquitous advanced polymers with multiple uses and applications.

Nucleophile-assisted racemisations of halosilanes - kinetic studies

Bassindale, Alan R.,Lau, Juliana C.-Y.,Taylor, Peter G.

, p. 75 - 82 (2007/10/02)

Kinetic studies have been carried out on the nucleophile-induced racemisation of PhMeCHSiMe2X, 2, X = triflate, Br or Cl.Thirteen nucleophiles were studied.The results are interpreted in terms of two competing mechanisms for racemisation: (a) nucleophile attack on a silane-nucleophile complex formed by displacement of the halide by the nucleophile, and (b) halide-halosilane exchange, with inversion of configuration.Solvent effects were examined, and kinetic orders in the nucleophile and in one case for the halosilane were determined.The order in added nucleophile varied between one and two, with strong nucleophiles in polar media.Anomalously high orders in nucleophile were observed in non-polar media and are ascribed to aggregation of the nucleophile.A kinetic analysis of the competing mechanisms was attempted, and was consistent with the experimental findings.In this particular series of reactions involving compounds with good leaving groups and relatively powerful nucleophiles there was no evidence for intermediates involving extracoordinate silicon. Keywords: Silicon; Racemisation; Mechanism

Nucleophile-assisted racemisation of halosilanes; an alternative pathway involving halide exchange

Bassindale, Alan R.,Lau, Juliana C.-Y.,Taylor, Peter G.

, p. 213 - 224 (2007/10/02)

An NMR method using diastereotopic halosilanes, PhCH(Me)SiMe2X (X = Cl or Br) has been developed for studying nucleophile-assisted racemisations of halosilanes.A mechanism for racemisation involving halide exchange is proposed to account for the observati

LE COMPLEXE 2> CATALYSEUR HOMOGENE D'HYDROGENATION ET D'HYDROSILYLATION D'OLEFINES ET D'ALDEHYDES ET CETONES α,β-INSATURES

Rumin, R.

, p. 351 - 356 (2007/10/02)

The chloro-bridged platinum(II) complex dichlorobis(2,4,6-trimethylpyridine)platinum was found to be an active catalyst for homogeneous hydrogenation and hydrosilylation of olefins and α,β-unsaturated aldehydes and ketones at room temperature and under atmospheric pressure.Hydrosilylation of terminal olefins can be achieved with dimethylphenylsilane and a catalyst/reactant ratio of 10-6/1.This complex is the first example of a platinum(II) compound containing pyridine ligands having good catalytic activity possibilities.

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