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Disiloxane, 1,3-diethoxy-1,3-dimethyl-1,3-diphenyl-, also known as 1,3-Diethoxy-1,3-dimethyl-1,3-diphenyldisiloxane, is a colorless liquid with the chemical formula C18H24O2Si2. It is a type of disiloxane, which is a cyclic siloxane compound consisting of two silicon atoms connected by an oxygen bridge. This specific disiloxane derivative features two ethoxy groups, two methyl groups, and two phenyl groups attached to the silicon atoms. It is used as a coupling agent, a release agent, and a component in various silicone-based products. Due to its unique structure and properties, it is widely employed in the fields of polymer chemistry, materials science, and pharmaceuticals.

4313-76-2

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4313-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4313-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,1 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4313-76:
(6*4)+(5*3)+(4*1)+(3*3)+(2*7)+(1*6)=72
72 % 10 = 2
So 4313-76-2 is a valid CAS Registry Number.

4313-76-2SDS

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 1,3-Diaethoxy-1,3-dimethyl-1,3-diphenyl-disiloxan

1.2 Other means of identification

Product number -
Other names 1.3-Diaethoxy-1.3-dimethyl-1.3-diphenyl-disiloxan

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:4313-76-2 SDS

4313-76-2Relevant academic research and scientific papers

METHOD FOR PRODUCING HALOSILANE

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Paragraph 0028; 0033; 0034, (2019/07/31)

PROBLEM TO BE SOLVED: To provide a method for producing halosilane that can efficiently produce halosilane. SOLUTION: Alkoxy halomethane is used as a halogenating agent and reacted with oxysilane having a structure represented by formula (a), to efficiently produce halosilane having a structure represented by formula (b) (In the formula (b), X is a chlorine atom, a bromine atom, or an iodine atom). SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

Conversion of hydrosilanes to alkoxysilanes catalyzed by Cp2TiCl2/nBuLi

Bedard, Thomas C.,Corey, Joyce Y.

, p. 315 - 333 (2007/10/02)

The combination of Cp2TiCl2 and nBuLi provides an effective catalyst for alcoholysis of the model silanes n-HexSiH3, PhMeSiH2, Ph2SiH2 and PhMe2SiH by ethanol, isopropanol, t-butyl alcohol and phenol.Increasing the steric bulk of the substituents on either the alcohol or the silane generally requires longer reaction periods and/or increasing temperature.All SiH bonds are converted to SiOEt groups by ethanol and a single SiH bond in secondary silanes and two SiH bonds in tertiary silanes are replaced by t-butyl alcohol.Diols including pinacol, 2,4-pentanediol and 2,5-hexanediol react with PhRSiH2 (R = Me, Ph) to give 1,3-dioxa-2-silacyclopentanes, -hexanes and -heptanes, respectively.Attempts to form caged structures by condensation of primary silanes and triols was unsuccessful.Hydrolysis of PhRSiH2 is promoted by Cp2TiCl2/n-BuLi and the siloxane is produced in quantitative yield when R = Ph and a mixture of linear disiloxanes and trisiloxanes in addition to cyclopolysilanes are produced when R = Me.Other protic reagents including acids, mercaptans, amines and enolizable ketones did not react.The effects of reaction parameters such as temperature, silane to catalyst ratio, solvent, transition metal and replacements for nBuLi were also determined.

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