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18546-93-5

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18546-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18546-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,4 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18546-93:
(7*1)+(6*8)+(5*5)+(4*4)+(3*6)+(2*9)+(1*3)=135
135 % 10 = 5
So 18546-93-5 is a valid CAS Registry Number.

18546-93-5SDS

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 hexyl-[hexyl(dimethyl)silyl]oxy-dimethylsilane

1.2 Other means of identification

Product number -
Other names 1,3-Di-<1'-hexyl>-tetramethyldisiloxan

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:18546-93-5 SDS

18546-93-5Downstream Products

18546-93-5Relevant articles and documents

-

Bank,H.M. et al.

, p. 792 - 794 (1964)

-

Olefin isomerization and hydrosilylation catalysis by lewis acidic organofluorophosphonium salts

Perez, Manuel,Hounjet, Lindsay J.,Caputo, Christopher B.,Dobrovetsky, Roman,Stephan, Douglas W.

supporting information, p. 18308 - 18310 (2014/01/06)

Organofluorophosphonium salts of the formula [(C6F 5)3-xPhxPF][B(C6F5) 4] (x = 0, 1) exhibit Lewis acidity derived from a low-lying σ* orbital at P opposite F. This acidity is evidenced by the reactions of these salts with olefins, which catalyze the rapid isomerization of 1-hexene to 2-hexene, the cationic polymerization of isobutylene, and the Friedel-Crafts-type dimerization of 1,1-diphenylethylene. In the presence of hydrosilanes, olefins and alkynes undergo efficient hydrosilylation catalysis to the alkylsilanes. Experimental and computational considerations of the mechanism are consistent with the sequential activation and 1,2-addition of hydrosilane across the unsaturated C-C bonds.

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