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octa(4-methylphenyl)octasilsesquioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19086-33-0

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19086-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19086-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,8 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19086-33:
(7*1)+(6*9)+(5*0)+(4*8)+(3*6)+(2*3)+(1*3)=120
120 % 10 = 0
So 19086-33-0 is a valid CAS Registry Number.

19086-33-0Upstream product

19086-33-0Relevant academic research and scientific papers

Cage octaphenylsilsesquioxane from cyclic tetrasiloxanetetraol and its sodium salt

Tateyama, Seiji,Kakihana, Yuriko,Kawakami, Yusuke

, p. 898 - 902 (2010)

Cage octasilsesquioxane with various substituents were obtained by the condensation reaction of various all-cis cyclic tetrasiloxanetetraol (R-T4-tetraol, R = phenyl, p-tolyl, i-butyl, naphthyl) with benzyltrimethylammonium hydroxide or tetrabutylammonium fluoride as a catalyst. Co-condensation of phenyl-T4-tetraol with phenyl-d5-T4-tetraol or with p-tolyl-T4-tetraol were found to proceed through reshuffling process evidenced by scrambling of the substituents. Pure octa(4-bromo-substituted phenyl)octasilsesquioxane was synthesized for the first time from tetra(4-bromo-substituted phenyl)tetrasiloxanetetraol sodium salt.

Octa, deca, and dodeca(4-nitrophenyl) cage silsesquioxanes via 4-trimethylsilylphenyl derivatives

Miyazato, Akio,Pakjamsai, Chitsakon,Kawakami, Yusuke

experimental part, p. 3239 - 3244 (2010/06/20)

Pure octa, deca, and dodeca(4-nitrophenyl) cage silsesquioxanes were obtained by regio-selective 4-nitration of octa, deca, and dodeca(4- trimethylsilylphenyl) cage silsesquioxanes via ipso-substitution of trimethylsilyl-phenyl bonds by fuming nitric acid. 3-Nitration of octa(4-methylphenyl)octasilesquioxane was also described. The starting octa(4-methyl-, 4-isopropyl- and 4-trimethylsilylphenyl)octasilsesquioxanes were selectively formed in 9-21% isolated yield in the presence of hydrochloric acid. Mixtures of octa, deca and dodecasilsesquioxanes, with decasilsesquioxane as the main component, were formed in the presence of tetrabutylammmonium fluoride as a catalyst. All the cage compounds could be separated mainly by crystallization. The Royal Society of Chemistry 2010.

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