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Tris(triphenylsiloxy)borane, also known as triphenylsilyl borate or (Ph3SiO)3B, is a boron-containing organosilicon compound with the chemical formula C36H30BO3Si3. It is a colorless, crystalline solid that is soluble in organic solvents and is widely used as a Lewis acid catalyst in various organic reactions, such as hydrosilylation, hydroboration, and Friedel-Crafts reactions. The compound is characterized by its strong electron-donating ability due to the presence of three triphenylsiloxy groups, which makes it a highly effective catalyst in promoting the formation of carbon-carbon and carbon-heteroatom bonds. Tris(triphenylsiloxy)borane is also known for its stability and low toxicity, making it a preferred choice in many chemical synthesis processes.

1111-47-3

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1111-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1111-47-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1111-47:
(6*1)+(5*1)+(4*1)+(3*1)+(2*4)+(1*7)=33
33 % 10 = 3
So 1111-47-3 is a valid CAS Registry Number.

1111-47-3Relevant academic research and scientific papers

MANUFACTURING METHOD OF BOROSILOXANE

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Paragraph 0020; 0021; 0022, (2018/11/22)

PROBLEM TO BE SOLVED: To provide an industrially advantageous manufacturing method of borosiloxane, which is important as an electrolyte additive of a lithium ion battery or the like. SOLUTION: There is provided a boron compound having Lewis acid with index acceptor number of the Lewis acid of 60 to 110. There is provided a manufacturing method of borosiloxane represented by R5nB(OSiR1R2R3)3-n or the like by reacting hydrosilane represented by R1R2R3SiH or R1R2R4SiOSiR1R2H and a boronic acid derivative represented by R5nB(OR6)3-n or the like in the presence of a catalyst such as Tris (pentafluorophenyl) borane. R1 to R3 and R5 are each independently C1 to 12 alkyl or C6 to 12 aryl, R4 and R6 are each independently C1 to 12 alkyl, C6 to 12 aryl or H, and n is an integer of 0 to 2. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPO&INPIT

Ruthenium-catalysed multicomponent synthesis of borasiloxanes

Chatterjee, Basujit,Gunanathan, Chidambaram

supporting information, p. 2515 - 2518 (2017/03/01)

We present the selective atom economical synthesis of borasiloxanes using a multi-component approach directly by the one-pot ruthenium catalysed reaction of boranes, silanes and water.

Triphenylsiloxy and Diphenylsiladioxy Derivatives of Boron

Bhardwaj, P. N.,Srivastava, G.

, p. 300 - 304 (2007/10/02)

Tris(triphenylsiloxy)borane, phenyl bis(triphenylsiloxy)borane, 2-triphenylsiloxy-1,3,2-dioxa-borolanes, -borinanes, -borole and -borin and diphenyl bis(1,3,3,2-dioxa-borolane-2-oxy)silanes have been synthesized by various routes and the reactivity of Si-O-B linkage has been compared with that of Ge-O-B and Sn-O-B linkages.Tris(triphenylsiloxy)-borane reacts with acetyic acid by cleavage of Si-O bond to give triphenylsilyl acetate and boric acid. 2-Triphenylsiloxy-1,3,2-benzodioxaborole forms 1:1 addition complexes with pyridine, triethylamine and aniline.Condensation of diphenylsilane diol with boric acid, tri(isopropoxy)borane or phenyldihydroxyborane yields cyclic derivatives.

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