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Silane, trimethyl[(1-methyl-2,2-diphenylethenyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51425-63-9

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51425-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51425-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51425-63:
(7*5)+(6*1)+(5*4)+(4*2)+(3*5)+(2*6)+(1*3)=99
99 % 10 = 9
So 51425-63-9 is a valid CAS Registry Number.

51425-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Trimethyl[(1-methyl-2,2-diphenylethenyl)oxy]silane

1.2 Other means of identification

Product number -
Other names 1,1-Diphenylaceton-enol-trimethylsilylether

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:51425-63-9 SDS

51425-63-9Downstream Products

51425-63-9Relevant academic research and scientific papers

Direct transformation of silyl enol ethers into functionalized allenes

Langer, Peter,Doering, Manfred,Seyferth, Dietmar,Goerls, Helmar

, p. 573 - 584 (2007/10/03)

The first elimination reactions of silyl enol ethers to lithiated allenes are reported. These reactions allow a direct transformation of readily available silyl enol ethers into functionalized allenes. The action of three to four equivalents of lithium di

SUR L'OBTENTION HAUTEMENT REGIO- ET STEREOSELECTIVED'ENOXYSILANES PAR ACTION DU BIS(TRIMETHYLSILYL)ACETAMIDE EN MILIEU HMPT SUR LESS DERIVES CARBONYLES ENOLISABLES

Dedier, James,Gerval, Pierre,Frainnet, Emile

, p. 183 - 198 (2007/10/02)

The authors describe a new and general method for the preparation of enoxysilanes by silylation of enolizable aldehydes and ketones by use of bis(trimethylsilyl)acetamide in HMPT, in the presence of very small quantities of sodium metal(or another basic a

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