6904-59-2 Usage
Siloxane
A class of silicon-containing organic compounds This term describes the general category of the compound, which is a type of siloxane.
Common in silicone-based products
Frequently used as a component This indicates that the compound is often found in products that contain silicone, a common material with various applications.
Acetate derivative of trisiloxanol
A specific type of modification This describes the chemical structure of the compound, which is derived from trisiloxanol and has an acetate group.
Chloro group attached
A specific functional group present This provides information about the presence of a chloro group in the compound's structure.
Used in production of silicones
Industrial application This highlights one of the primary uses of the compound, which is in the manufacturing of silicone products.
Utilized in lubricants, adhesives, and coatings
Diverse applications This lists some of the specific products that may contain the compound.
Potential health and environmental hazards
Safety concerns This serves as a cautionary note about the possible risks associated with the compound, emphasizing the importance of proper handling and safety precautions.
Check Digit Verification of cas no
The CAS Registry Mumber 6904-59-2 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 6904-59:
(6*6)+(5*9)+(4*0)+(3*4)+(2*5)+(1*9)=112
112 % 10 = 2
So 6904-59-2 is a valid CAS Registry Number.
6904-59-2Relevant 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)>.
