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Silane, (1,1-dimethylethyl)(2-methoxyphenoxy)dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120951-84-0

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120951-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120951-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,5 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120951-84:
(8*1)+(7*2)+(6*0)+(5*9)+(4*5)+(3*1)+(2*8)+(1*4)=110
110 % 10 = 0
So 120951-84-0 is a valid CAS Registry Number.

120951-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl(2-methoxyphenoxy)dimethylsilane

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:120951-84-0 SDS

120951-84-0Relevant academic research and scientific papers

Efficient and chemoselective protection of alcohols and phenols with tert-butyldimethylchlorosilane (TBDMCS) under solvent-free conditions

Firouzabadi, Habib,Etemadi, Shahrad,Karimi, Babak,Jarrahpour, Ali Asghar

, p. 45 - 51 (1998)

Various types of primary and secondary alcohols and phenols can be converted efficiently to their corresponding TBDMS ethers using TBDMCS/imidazole under solvent-free conditions. Elimination of DMF, accompanied with an easy non-aqueous work-up and a high rate enhancement of the reaction are worthy to be mentioned for the presented method. The reactions show absolute chemoselectivity for the protection of primary in the presence of secondary alcohols.

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