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Acetoxydimethylvinylsilane, also known as (2-acetoxyethenyl)trimethylsilane, is an organosilicon compound with the chemical formula C6H12O2Si. It is a colorless liquid with a density of 0.92 g/cm3 and a boiling point of 58-60°C. acetoxydimethylvinylsilane is primarily used as a coupling agent in the production of composite materials, enhancing the adhesion between inorganic fillers and organic polymers. It is also employed as a silylating agent in organic synthesis, particularly in the formation of silyl ethers and other organosilicon derivatives. Acetoxydimethylvinylsilane is known for its stability and reactivity, making it a valuable intermediate in various chemical processes.

3293-09-2

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3293-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3293-09-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3293-09:
(6*3)+(5*2)+(4*9)+(3*3)+(2*0)+(1*9)=82
82 % 10 = 2
So 3293-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2Si/c1-5-9(3,4)8-6(2)7/h5H,1H2,2-4H3

3293-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [ethenyl(dimethyl)silyl] acetate

1.2 Other means of identification

Product number -
Other names EINECS 221-955-1

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:3293-09-2 SDS

3293-09-2Relevant academic research and scientific papers

Acyl iodides in organic synthesis: IX. Cleavage of the Si-O-C and Si-O-Si moieties

Voronkov,Trukhina,Belousova,Kuznetsova,Vlasova

, p. 501 - 506 (2007)

Reactions of acyl iodides RCOI (R = Me, Ph) with organosilicon compounds involve cleavage of the Si-O-C and Si-O-Si fragments. Acetyl iodide reacts with alkyl(alkoxy)silanes with evolution of heat, and cleavage of the Si-O bond results in the formation of oligo-or polysiloxanes, alkyl iodides, and alkyl acetates. 1,3-Diacetoxytetramethyldisiloxane is formed in the reaction of acetyl iodide with dimethoxy(dimethyl)silane. Acyl iodides readily react with 1-ethoxysilatrane to give 1-acyloxysilatranes as a result of cleavage of the C-O bond. The reaction of acetyl iodide with hexaethyldisiloxane yields triethylsilyl acetate and triethyliodosilane, while in the reaction with octamethyltrisiloxane iodo(trimethyl)silane and dimethyl(trimethylsiloxy)silyl acetate are obtained. Nauka/Interperiodica 2007.

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