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dimethyl(phenyl)((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)oxy)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1349697-23-9

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1349697-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1349697-23-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,9,6,9 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1349697-23:
(9*1)+(8*3)+(7*4)+(6*9)+(5*6)+(4*9)+(3*7)+(2*2)+(1*3)=209
209 % 10 = 9
So 1349697-23-9 is a valid CAS Registry Number.

1349697-23-9Downstream Products

1349697-23-9Relevant articles and documents

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

, p. 9998 - 10001 (2017)

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.

Preparation method of borosiloxane compound

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Paragraph 0019-0020; 0025-0028, (2021/06/21)

The invention discloses a preparation method of a borosiloxane compound. The preparation method comprises the following steps: 1) with borane, silane and water as starting raw materials, adding a photosensitizer and an organic solvent into a reaction container, carrying out a stirring reaction under the irradiation of blue light, and stopping stirring when it is detected that the reaction raw material borane completely disappears through in gas chromatographic detection so as to obtain a reaction solution; and 2) removing a volatile solvent from the reaction solution, conducting extracting with n-hexane, dehydrating and drying an obtained organic phase with anhydrous sodium sulfate, and conducting concentrating under reduced pressure to obtain the target product. According to the method for preparing borosiloxane, traditional precious metal catalysis is replaced with blue light catalysis for the first time; borane, silane and water are used as raw materials, the reaction occurs along with release of molecular hydrogen, atom economy is high, waste is avoided, so production cost is greatly reduced, and remarkable social benefits and economic benefits are achieved; and in addition, the method is mild in catalysis conditions, simple in catalysis system, high in reaction selectivity, high in safety, high in synthesis efficiency and worthy of popularization and application.

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

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

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.

Nanogold-catalyzed cis -silaboration of alkynes with abnormal regioselectivity

Gryparis, Charis,Stratakis, Manolis

supporting information, p. 1430 - 1433 (2014/04/03)

The first example of gold-catalyzed silaboration of alkynes with PhMe 2SiBpin is documented in the presence of supported gold nanoparticles. In the case of terminal alkynes, the reaction proceeds at ambient conditions in very good yields and th

Copper-mediated reduction of CO2 with pinB-SiMe2Ph via CO2 insertion into a copper-silicon bond

Kleeberg, Christian,Cheung, Man Sing,Lin, Zhenyang,Marder, Todd B.

, p. 19060 - 19063 (2012/01/12)

Reaction of [(IPr)Cu-OtBu] (1) with pinB-SiMe2Ph (2) leads to the Cu-silyl complex [(IPr)Cu-SiMe2Ph] (3). Insertion of CO 2 into the Cu-Si bond of 3 is followed by transformation of the resulting silanecarboxy complex [(IP

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