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1,3,5,7,9-pentaethylcyclopentasiloxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17995-44-7

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17995-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17995-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,9 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17995-44:
(7*1)+(6*7)+(5*9)+(4*9)+(3*5)+(2*4)+(1*4)=157
157 % 10 = 7
So 17995-44-7 is a valid CAS Registry Number.

17995-44-7Downstream Products

17995-44-7Relevant academic research and scientific papers

Unexpected reactions of dichloro(ethyl)silane with DMSO in organic solvents

Basenko,Maylyan

, p. 903 - 907 (2017/09/29)

The effect of the solvent nature on the composition of the products formed upon the reaction between EtSi(H)Cl2 and DMSO (molar ratio 1: 1, 0 °C) was revealed. This reaction in non-polar and low polar solvents (toluene, chloroform) gives oligoethyl(hydro)cyclo-siloxanes ((EtSi(H)O)n, n = 3—8) as the major products in the yields up to 77%. In MeCN, oligoethyl(hydro)cyclosiloxanes are formed along with cyclic monochlorinated siloxanes ((EtSi(H)O)n(EtSi(Cl)O), n = 2—7) in a ratio of ~7: 3 (68: 29 wt.%). In excess diethyl ether, the overall yield of oligoethyl(hydro)cyclosiloxanes does not exceed 25% and the major products are linear α,ω-diethoxyoligoethyl(hydro)siloxanes (EtO(EtSi(H)O)nEt, n = 2—7) formed in 70—75% yields. A plausible reaction mechanism leading to the final products was suggested. Apparently, the reaction proceeds via ethyl(hydro)-and chloro(ethyl)silanones as intermediates.

FEATURES OF INFLUENCE OF HCl ON HYDROLYTIC COPOLYCONDENSATION OF BIFUNCTIONAL ORGANOCHLOROSILANES WITH TRIMETHYLCHLOROSILANE

Kopylov, V. M.,Agashkov, S. P.,Sunkovich, G. V.,Prikhod'ko, P. L.

, p. 1257 - 1261 (2007/10/02)

The hydrogen chloride that is formed in the hydrolytic copolycondensation of R'RSiCl2 with Me3SiCl affects the composition of the reaction products only at cocentrations above 30-35percent, where it is responsible for splitting out the terminal trimethylsiloxy group.The stability of the terminal groups increases with increasing size of the substituents on the silicon atom in the R'RSiCl2.The total yield of Me3SiO(R'RSiO)mSiMe3 with m = 1-4 also increases with increasing size of the substituents on the silicon atom in the R'RSiCl2.The total yield of p with p = 3-5 increases with decreasing tendency of the R'RSiCl2 to form rings by hydrolytic polycondensation, and with increasing sensitivity of the terminal trimethylsiloxy group in the cocondensation products to the action of HCl and its activity with respect to the siloxane bond.

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