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(E)-4,4,5,5-tetramethyl-2-(1-phenylhex-4-en-3-yl)-1,3,2-dioxaborolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1373170-55-8

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1373170-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373170-55-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,1,7 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1373170-55:
(9*1)+(8*3)+(7*7)+(6*3)+(5*1)+(4*7)+(3*0)+(2*5)+(1*5)=148
148 % 10 = 8
So 1373170-55-8 is a valid CAS Registry Number.

1373170-55-8Relevant academic research and scientific papers

Practical Synthesis of Allyl, Allenyl, and Benzyl Boronates through SN1′-Type Borylation under Heterogeneous Gold Catalysis

Miura, Hiroki,Hachiya, Yuka,Nishio, Hidenori,Fukuta, Yohei,Toyomasu, Tomoya,Kobayashi, Kosa,Masaki, Yosuke,Shishido, Tetsuya

, p. 758 - 766 (2021/02/03)

Efficient borylation of sp3 C-O bonds by supported Au catalysts is described. Au nanoparticles supported on TiO2 showed high activity under mild conditions employing low catalyst loading conditions without the aid of any additives, such as phosphine and bases. A variety of allyl, propargyl, and benzyl substrates participated in the heterogeneously catalyzed reactions to furnish the corresponding allyl, allenyl, and benzyl boronates in high yields. Besides, Au/TiO2 was also effective for the direct borylation of allylic and benzylic alcohols. A mechanistic investigation based on a Hammett study and control experiments revealed that sp3 C-O bond borylation over supported Au catalysts proceeded through SN1′-type mechanism involving the formation of a carbocationic intermediate. The high activity, reusability, and environmental compatibility of the supported Au catalysts as well as the scalability of the reaction system enable the practical synthesis of valuable organoboron compounds.

Highly diastereoselective and enantiospecific allylation of ketones and imines using borinic esters: Contiguous quaternary stereogenic centers

Chen, Jack L.-Y.,Aggarwal, Varinder K.

supporting information, p. 10992 - 10996 (2015/03/30)

3,3-Disubstituted allylic boronic esters are not sufficiently reactive to react with ketones and imines. However they can be converted into the corresponding borinic esters by the sequential addition of nBuLi and TFAA. These reactive intermediates possess

Practical procedure for copper(I)-catalyzed allylic boryl substitution with stoichiometric alkoxide base

Ito, Hajime,Miya, Takanori,Sawamura, Masaya

scheme or table, p. 3423 - 3427 (2012/06/15)

We have developed a useful procedure for borylation using catalytic CuCl/Xantphos and stoichiometric K(O-t-Bu): the highly versatile method is suitable for the synthesis of allylboronates including those with terminal and internal allylic systems, cyclic

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