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Acetic acid, (triphenylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18666-58-5

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18666-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18666-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,6 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18666-58:
(7*1)+(6*8)+(5*6)+(4*6)+(3*6)+(2*5)+(1*8)=145
145 % 10 = 5
So 18666-58-5 is a valid CAS Registry Number.

18666-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-triphenylsilylacetic acid

1.2 Other means of identification

Product number -
Other names triphenylsilylacetic acid

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:18666-58-5 SDS

18666-58-5Relevant academic research and scientific papers

Electrochemical synthesis of 1,2-disilylethanes from α-silylacetic acids

Shtelman, Alex V.,Becker, James Y.

, p. 4710 - 4714 (2011/07/08)

The synthesis of 1,2-disilylethanes [R1R2R 3Si(CH2)2SiR1R2R 3] is usually conducted by using noble metal reagents or catalysts. This work describes a new electrochemical synthetic method for their preparation in good yields by oxidation of α-silylacetic acids at Pt anodes (Kolbe electrolysis). Most of the reported synthesized 1,2-disilylethanes in this work are unknown.

A convenient method for the synthesis of α-silylacetic acids

Shtelman, Alex V.,Becker, James Y.

, p. 3101 - 3103 (2008/09/20)

A method is described for the preparation of α-silylacetic acids of the type R3SiCH2CO2H by treating trimethylsilyl acetate with LDA followed by quenching with chlorosilanes.

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