5314-58-9 Usage
General Description
1,3-Diacetoxytetramethyldisiloxane is a chemical compound with the molecular formula C10H22O4Si2. It is a colorless and odorless liquid that is commonly used as a coupling agent and cross-linking agent in various industries, including the production of silicone polymers and coatings. It is also utilized as a reagent in organic synthesis, particularly in the formation of carbon-silicon bonds. 1,3-Diacetoxytetramethyldisiloxane has low toxicity and is considered to be relatively safe for handling and use, although proper precautions should still be taken to prevent exposure and potential health hazards. Additionally, it is important to note that 1,3-Diacetoxytetramethyldisiloxane should be stored and handled in accordance with relevant safety regulations and guidelines to ensure safe and proper usage.
Check Digit Verification of cas no
The CAS Registry Mumber 5314-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5314-58:
(6*5)+(5*3)+(4*1)+(3*4)+(2*5)+(1*8)=79
79 % 10 = 9
So 5314-58-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O5Si2/c1-7(9)11-14(3,4)13-15(5,6)12-8(2)10/h1-6H3
5314-58-9Relevant articles and documents
Ir-catalyzed hydrosilylation reaction of allyl acetate with octakis(dimethylsiloxy)octasilsesquioxane and related hydrosilanes
Igarashi, Masayasu,Matsumoto, Tomohiro,Kobayashi, Toshiaki,Sato, Kazuhiko,Ando, Wataru,Shimada, Shigeru,Hara, Masanao,Uchida, Hiroshi
, p. 141 - 146 (2014/01/17)
Hydrosilylation reaction of allyl acetate (AA) with octakis(dimethylsiloxy) octasilsesquioxane [(HSiMe2O)8(SiO1.5) 8] was efficiently catalyzed by chloro(1,5-cyclooctadiene)iridium(I) dimer [Ir(μ-Cl)(COD)]2
REACTIONS IN THE CHLOROSILANE-SILANOL-SILOXANE SYSTEM
Ruehlmann, K.
, p. 139 - 152 (2007/10/02)
We obtained the first ?*-values and ES-values for siloxy groups by spectroscopic and kinetic methods.Detailed mechanistic investigations are performed on the hydrolysis of chlorosilanes, the cleavage of Si-O-Si bonds by HCl, and the substituent exchange reaction between silanols and chlorosilanes.
