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Silanol, triphenyl-, acetate is a complex organic compound with the chemical formula C26H23O3Si. It is derived from silanol, a silicon analog of alcohol, and features a triphenyl group (three phenyl rings) attached to the silicon atom. The acetate group is bonded to the silicon, forming an ester linkage. Silanol, triphenyl-, acetate is primarily used in the field of organic synthesis, particularly in the preparation of various organosilicon compounds. It is known for its stability and reactivity, which makes it a valuable intermediate in the synthesis of silicones and other silicon-containing materials. The compound's structure and properties make it suitable for applications in materials science, pharmaceuticals, and specialty chemicals.

1929-33-5

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1929-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1929-33-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1929-33:
(6*1)+(5*9)+(4*2)+(3*9)+(2*3)+(1*3)=95
95 % 10 = 5
So 1929-33-5 is a valid CAS Registry Number.

1929-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,hydroxy(triphenyl)silane

1.2 Other means of identification

Product number -
Other names Essigsaeure-triphenylsilylester

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:1929-33-5 SDS

1929-33-5Relevant academic research and scientific papers

Acyl iodides in organic synthesis. Reaction of acyl iodides with triphenylethoxy- and triphenylhydroxysilane

Voronkov,Tsyrendorzhieva,Rakhlin

experimental part, p. 1621 - 1622 (2010/04/27)

The reaction of triphenylethoxysilane with acetyl or benzoyl iodide led to the formation of triphenyliodosilane and ethyl ester of the corresponding carboxylic acid. Triphenyliodosilane formed also in the reaction of triphenylsilanol with benzoyl iodide.

Metallkomplexe in Anorganichen Matrices, 5. Katalytische Silanoxidation an einem heterogenisierten Rhodium-Komplex

Egger, Christian,Schubert, Ulrich

, p. 783 - 788 (2007/10/02)

A heterogenized rhodium complex, prepared by sol-gel processing of Rh(CO)Cl2 and Si(OEt)4, is shown to catalyze the conversion of the silanes H4-nSiPhn (n = 1-3) or (HMe2Si)2O to (poly)siloxanes by air or water.Using THF as a solvent, the silanoles Ph3SiOH or Ph2Si(OH)2 are obtained instead.The reaction of phenylacetic acid or acetic acid with HSiPh3 to give silyl esters is catalyzed by the same compound.

REDUCTIVE DEOXYGENATION OF ALCOHOLS VIA ESTERS WITH TRIPHENYLSILANE UNDER NEUTRAL CONDITIONS

Sano, Hiroshi,Ogata, Mayako,Migita, Toshihiko

, p. 77 - 80 (2007/10/02)

Treatment of carboxylic esters derived from alcohols with triphenylsilane in the presence of a radical generator at 140 deg C gave the corresponding hydrocarbons in good yield.

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