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2117-43-3

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2117-43-3 Usage

Structure

Silacyclohexane ring with two oxygen atoms at positions 1 and 3, and two phenyl groups attached to the silicon atom at position 2.

Functionality

Building block for the synthesis of more complex organosilicon compounds and materials.

Applications

Organic and materials chemistry, development of new functional materials, precursor for silicon-containing polymers with specialized properties.

Unique Features

Interesting and promising compound for further research and development due to its structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 2117-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2117-43:
(6*2)+(5*1)+(4*1)+(3*7)+(2*4)+(1*3)=53
53 % 10 = 3
So 2117-43-3 is a valid CAS Registry Number.

2117-43-3SDS

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 2,2-diphenyl-1,3,2-dioxasilinane

1.2 Other means of identification

Product number -
Other names 1,3-Dioxa-2-silacyclohexane,2,2-diphenyl

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:2117-43-3 SDS

2117-43-3Downstream Products

2117-43-3Relevant articles and documents

An Efficient Catalyst for the Conversion of Hydrosilanes to Alkoxysilanes

Lorenz, Catrin,Schubert, Ulrich

, p. 1267 - 1270 (2007/10/03)

The copper(I) hydride 6 is an efficient catalyst for the alcoholysis of primary and secondary silanes.The reactions proceed at room temperature within a few hours and give the alkoxysilanes in high yields.Only with bulky alcohols or silanes are longer reaction times and/or increased temperatures required.The presence of air accelarates the reactions and gives rise to higher yields of alkoxysilanes, particularly with bulky alcohols.Diols react with PhRSiH2 (R = Me, Ph) to afford 1,3-dioxo-2-silacycloalkanes and with tertiary silanes to furnish the bissilylated diols.When unsaturated alcohols (2-propen-1-ol or 2-propyn-1-ol) are employed, the double or triple bond is retained. - Keywords: Catalytic silane alcoholysis; Alkoxysilanes

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