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Silane, triethyl[[1-(2-phenylethyl)-3-butenyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183955-08-0

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183955-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183955-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,9,5 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 183955-08:
(8*1)+(7*8)+(6*3)+(5*9)+(4*5)+(3*5)+(2*0)+(1*8)=170
170 % 10 = 0
So 183955-08-0 is a valid CAS Registry Number.

183955-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl(1-phenylhex-5-en-3-yloxy)silane

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:183955-08-0 SDS

183955-08-0Relevant academic research and scientific papers

Diastereoselective synthesis of trifluoromethylated 1,3-dioxanes by intramolecular oxa-Michael reaction

Becerra-Figueroa, Liliana,Brun, Elodie,Mathieson, Michael,Farrugia, Louis J.,Wilson, Claire,Prunet, Jo?lle,Gamba-Sánchez, Diego

supporting information, p. 301 - 305 (2017/01/13)

A highly diastereoselective synthesis of trifluoromethylated 1,3-dioxanes is described. The reaction proceeds by an addition/oxa-Michael sequence and works efficiently under mild reaction conditions, with a good substrate scope and acceptable to good yiel

A New, Simple, and Selective Palladium-Catalyzed Cleavage of Triethylsilyl Ethers

Rotulo-Sims, Delphine,Prunet, Joelle

, p. 4701 - 4704 (2007/10/03)

(Equation Presented) A simple procedure for the cleavage of triethylsilyl (TES) ethers in the presence of 10 wt % Pd/C in methanol or 95% ethanol is reported. This method allows selective removal of alkyl TES ethers in the presence of aromatic TES ethers or tert-butyldimethylsilyl (TBS) protecting groups.

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