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Triphenyl((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxy)silane is a complex organic compound with the molecular formula C25H31BO4Si. It is a colorless solid that is soluble in organic solvents. triphenyl((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxy)silane is a derivative of triphenylsilane, featuring a 1,3,2-dioxaborolane group attached to the oxygen atom. The 1,3,2-dioxaborolane group is a synthetically useful moiety, often used in Suzuki-Miyaura cross-coupling reactions, a type of carbon-carbon bond-forming reaction in organic chemistry. The compound's structure consists of a silicon atom bonded to three phenyl groups and an oxygen atom, which in turn is connected to the 1,3,2-dioxaborolane group. This specific arrangement endows the compound with unique reactivity and stability, making it a valuable intermediate in the synthesis of various organosilicon compounds and other complex organic molecules.

82172-54-1

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82172-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82172-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82172-54:
(7*8)+(6*2)+(5*1)+(4*7)+(3*2)+(2*5)+(1*4)=121
121 % 10 = 1
So 82172-54-1 is a valid CAS Registry Number.

82172-54-1Relevant academic research and scientific papers

METHOD FOR PRODUCING BORYL SILYL ETHER

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Paragraph 0025-0027, (2018/09/26)

PROBLEM TO BE SOLVED: To provide a method for producing boryl silyl ether that can efficiently produce boryl silyl ether. SOLUTION: In the presence of a catalyst containing a group 10 element and/or a group 11 element in the periodic table, the reaciton between silanol and diborane makes it possible to produce efficiently boryl silyl ether. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPO&INPIT

Synthesis of borasiloxanes by oxidative hydrolysis of silanes and pinacolborane using Cu3(BTC)2 as a solid catalyst

Dhakshinamoorthy, Amarajothi,Asiri, Abdullah M.,Concepcion, Patricia,Garcia, Hermenegildo

supporting information, p. 9998 - 10001 (2017/09/12)

A convenient method for the synthesis of borasiloxanes from silanes and pinacolboranes using Cu3(BTC)2 as a heterogeneous catalyst in acetonitrile at 70 °C is reported. This procedure is more convenient than Ru and Pd based homogeneous catalysts because it avoids the use of noble metals, easy handling of starting materials and the catalyst can be reused.

A convenient and clean synthetic method for borasiloxanes by Pd-catalysed reaction of silanols with diborons

Yoshimura, Aya,Yoshinaga, Michiyo,Yamashita, Hiroshi,Igarashi, Masayasu,Shimada, Shigeru,Sato, Kazuhiko

supporting information, p. 5822 - 5825 (2017/07/11)

Selective O-borylation of silanols with diborons took place in the presence of Pd catalysts to give the corresponding boryl silyl ethers in high yields.

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.

Selective boryl silyl ether formation in the photoreaction of bisboryloxide/boroxine with hydrosilane catalyzed by a transition-metal carbonyl complex

Ito, Masaki,Itazaki, Masumi,Nakazawa, Hiroshi

supporting information, p. 6183 - 6186 (2014/05/20)

Selective B-O-Si bond formation was achieved in the reaction of bisboryloxide O(Bpin)2 (pin = (OCMe2)2)/ boroxine (MeBO)3 system with tertiary silane R3SiH in the presence of stoichiometric water and a catalytic amount of [M](CO)5 ([M] = Mo(CO), W(CO), Fe) to give boryl silyl ethers. Moreover, this reaction can be applied to various hydrosilanes (disilyl compounds and secondary silanes) and hydrogermane. Some of the boryl silyl ethers thus formed were confirmed by X-ray analysis.

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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