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Disiloxanol, 3-chloro-1,1,3,3-tetramethyl-, acetate is a complex organic compound with the chemical formula C8H19ClO2Si2. It is a derivative of disiloxanol, which is a type of siloxane, a class of compounds containing silicon and oxygen atoms. This specific compound features a 3-chloro-1,1,3,3-tetramethyl disiloxanol moiety, which is esterified with acetic acid. The presence of the chlorine atom and the acetate group gives Disiloxanol, 3-chloro-1,1,3,3-tetramethyl-, acetate unique properties, making it useful in various chemical applications, such as in the synthesis of silicone-based materials and as a potential intermediate in the production of specialty chemicals. Its structure and reactivity are influenced by the presence of the silicon-oxygen bonds and the chlorinated and esterified functional groups, which can participate in various chemical reactions.

6904-58-1

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6904-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6904-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6904-58:
(6*6)+(5*9)+(4*0)+(3*4)+(2*5)+(1*8)=111
111 % 10 = 1
So 6904-58-1 is a valid CAS Registry Number.

6904-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-acetoxy-3-chlorotetramethyldisiloxane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6904-58-1 SDS

6904-58-1Relevant academic research and scientific papers

REACTION OF OCTAMETHYLCYCLOTETRASILOXANE AND PERMETHYLOLIGOSILOXANES WITH ACYL CHLORIDES IN THE PRESENCE OF CoCl2

Basenko, S. V.,Ogorodnikova, E. I.,Vitkovskii, V. Yu.,Mirskov, R. G.,Voronkov, M. G.

, p. 79 - 83 (2007/10/02)

Octamethylcyclotetrasiloxane is cleaved quantitatively by acetyl chloride (1:1 molar ratio) in the presence of anhydrous CoCl2 in acetonitrile at room temperature to form primarily α-chloro-ω-acetoxyoligodimethylsiloxanes nOCOCH3 (n = 0-3; yield, 60-65percent)>.In the presence of an equimolar amount of trimethylacetoxysilane of hexamethyldisiloxane, the major reaction products are α-methyl-ω-acetoxyoligodimethylsiloxanes nOCOCH3 (n = 4-6; yield, 65-70percent)>.

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