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Tris(tert.-butylphenyl)-cyclo-trisiloxane is a cyclic organosilicon compound with the chemical formula C30H45Si3O3. It consists of a cyclic structure containing three silicon atoms and three oxygen atoms, with each silicon atom bonded to a tert-butylphenyl group. tris(tert.-butylphenyl)-cyclo-trisiloxane is known for its thermal stability, low toxicity, and excellent resistance to UV radiation, making it a valuable component in various applications such as high-performance polymers, adhesives, sealants, and coatings. Its unique structure also contributes to its low surface energy, which can be beneficial in reducing adhesion and improving the release properties of certain materials.

75355-53-2

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75355-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75355-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,5 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75355-53:
(7*7)+(6*5)+(5*3)+(4*5)+(3*5)+(2*5)+(1*3)=142
142 % 10 = 2
So 75355-53-2 is a valid CAS Registry Number.

75355-53-2Downstream Products

75355-53-2Relevant academic research and scientific papers

Lithium Fluorosilanolates - Units of Chain and Ring Siloxanes

Klingebiel, Uwe

, p. 3366 - 3371 (2007/10/02)

Potassium hydroxide reacts with difluorosilanes R-SiF2-R' (1 - 4: R = R' = CMe3, NC2H5(SiMe3), N-iC3H7(SiMe3); R = CMe3, R' = C6H5) to give the fluorosilanols R-FSiOH-R' (7 - 10).The siloxane is obtained in the reaction of SiF2 (6) with KOH via a 1,3-silyl group migration. 7 - 10 react with butyllithium to give the lithium fluorosilanolates 11 - 14.The reaction of these lithium salts with halogensilanes leads to the formation of the halogen functional siloxanes 15, 17 - 21.Lithiated 16 (22) is substituted by fluorosilanes at the nitrogen (23 - 25).The cyclic siloxanes 26 - 28 are formed by thermal LiF elimination from 11 and 12.Dilithiated di-tert-butylsilanol reacts with 15 to give 2,2,4,6-tetra-tert-butyl-4,6-diphenylcyclotrisiloxane (29).

SYNTHESE VON FLUORSILYLOXIMEN

Bentmann, D.,Klingebiel, U.

, p. 519 - 526 (2007/10/02)

Fluorosilanes react with lithium salts of acyclic and cyclic oximes, eliminating LiF and forming O-fluorosilyloximes and O,O'-fluorosilyldioximes in a molar ratio 1 : 2.The N-O bond is cleaved in the reaction of O-fluorosilyloximes with butyllithium.Bis(t

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