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Silane, triethyl(2-methoxyphenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18406-12-7

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18406-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18406-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,0 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18406-12:
(7*1)+(6*8)+(5*4)+(4*0)+(3*6)+(2*1)+(1*2)=97
97 % 10 = 7
So 18406-12-7 is a valid CAS Registry Number.

18406-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl-(2-methoxy-phenoxy)-silane

1.2 Other means of identification

Product number -
Other names 1-Triaethylsiloxy-2-methoxybenzol

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:18406-12-7 SDS

18406-12-7Relevant academic research and scientific papers

Mild synthesis of silyl ethers: Via potassium carbonate catalyzed reactions between alcohols and hydrosilanes

Delucia, Nicholas A.,Das, Nivedita,Vannucci, Aaron K.

, p. 3415 - 3418 (2018)

A method has been developed for the silanolysis of alcohols using an abundant and non-corrosive base K2CO3 as a catalyst. Reactions between a variety of alcohols and hydrosilanes generate silyl ethers under mild conditions. The use of hydrosilanes leads to the formation of H2 as the only byproduct thus avoiding the formation of stoichiometric strong acids. The mild conditions lead to a wide scope of possible alcohol substrates and good functional group tolerance. Selective alcohol silanolysis is also observed in the presence of reactive C-H bonds, lending this method for extensive use in protection group chemistry.

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