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17938-09-9

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17938-09-9 Usage

General Description

1,3-Diphenyl tetramethoxy disiloxane is a chemical compound with the molecular formula C20H30O4Si2. It is a siloxane derivative with two silicon atoms, four methoxy groups, and two phenyl groups. 1,3 DIPHENYL TETRAMETHOXY DISILOXANE is commonly used as a reagent and intermediate in organic synthesis, especially in the production of silicon-related compounds. It is also used in the manufacturing of polymers and as a coating agent for various materials. 1,3-Diphenyl tetramethoxy disiloxane is known for its high thermal stability and resistance to oxidation, making it a valuable compound in industrial applications. Additionally, it is a colorless, odorless liquid with low solubility in water but good solubility in organic solvents.

Check Digit Verification of cas no

The CAS Registry Mumber 17938-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,3 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17938-09:
(7*1)+(6*7)+(5*9)+(4*3)+(3*8)+(2*0)+(1*9)=139
139 % 10 = 9
So 17938-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H22O5Si2/c1-17-22(18-2,15-11-7-5-8-12-15)21-23(19-3,20-4)16-13-9-6-10-14-16/h5-14H,1-4H3

17938-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [dimethoxy(phenyl)silyl]oxy-dimethoxy-phenylsilane

1.2 Other means of identification

Product number -
Other names [PhSi(OMe)2]2O

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:17938-09-9 SDS

17938-09-9Relevant articles and documents

Practical conversion of chlorosilanes into alkoxysilanes without generating HCl

Wakabayashi, Ryutaro,Sugiura, Yasushi,Shibue, Toshimichi,Kuroda, Kazuyuki

supporting information; experimental part, p. 10708 - 10711 (2011/12/05)

Alcohol-free: A versatile, efficient, and practical synthesis of alkoxysilanes without generation of HCl involves the reaction of chlorosilanes with unsymmetrical ethers in the presence of a Lewis acid (see scheme). The reaction proceeds through selective cleavage of C-O bonds and is superior to conventional processes. Industrially feasible reagents are used and only one by-product results. Copyright

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