154820-97-0 Usage
Uses
Used in Organic Synthesis:
5-PHENYL-1-PENTENYLBORONIC ACID PINACOL ESTER is used as a reagent for the formation of carbon-carbon bonds in organic synthesis, facilitating the creation of complex organic molecules.
Used in Suzuki-Miyaura Coupling Reactions:
In the field of organic chemistry, 5-PHENYL-1-PENTENYLBORONIC ACID PINACOL ESTER is used as a coupling partner in Suzuki-Miyaura reactions, a widely employed method for the synthesis of biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
5-PHENYL-1-PENTENYLBORONIC ACID PINACOL ESTER is used as a building block in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
5-PHENYL-1-PENTENYLBORONIC ACID PINACOL ESTER is utilized as an intermediate in the preparation of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals to improve crop protection and yield.
Used in Materials Science:
5-PHENYL-1-PENTENYLBORONIC ACID PINACOL ESTER is employed in materials science applications, where it contributes to the synthesis of advanced materials with specific properties, such as conductivity, stability, or optical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 154820-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,8,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 154820-97:
(8*1)+(7*5)+(6*4)+(5*8)+(4*2)+(3*0)+(2*9)+(1*7)=140
140 % 10 = 0
So 154820-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H25BO2/c1-16(2)17(3,4)20-18(19-16)14-10-6-9-13-15-11-7-5-8-12-15/h5,7-8,10-12,14H,6,9,13H2,1-4H3/b14-10+
154820-97-0Relevant academic research and scientific papers
Cyclic (Alkyl)(amino)carbene Ligands Enable Cu-Catalyzed Markovnikov Protoboration and Protosilylation of Terminal Alkynes: A Versatile Portal to Functionalized Alkenes**
Bertrand, Guy,Engle, Keary M.,Gao, Yang,Grotjahn, Douglas B.,Jazzar, Rodolphe,Junor, Glen P.,Kang, Taeho,Kendrick, Aaron,Yazdani, Sima
supporting information, p. 19871 - 19878 (2021/08/13)
Regioselective hydrofunctionalization of alkynes represents a straightforward route to access alkenyl boronate and silane building blocks. In previously reported catalytic systems, high selectivity is achieved with a limited scope of substrates and/or rea
Coupling of Trifluoroacetaldehyde N-Triftosylhydrazone with Organoboronic Acids for the Synthesis of gem-Difluoroalkenes
Ma, Yu,Reddy, Bhoomireddy Rajendra Prasad,Bi, Xihe
supporting information, p. 9860 - 9863 (2019/12/24)
The synthesis of alkyl gem-difluoroalkenes remains a difficult task in organic synthesis. Here, we report a general and efficient approach for tackling this problem by gem-difluoroolefination of trifluoroacetaldehyde N-triftosylhydrazone with organoboronic acids. This protocol is operationally simple, free of transition metals, and suitable for a broad range of organoboronic acids. Moreover, the utility of the products was demonstrated by further conversion of the gem-difluorovinyl group.
Synthesis of 1,1-organodiboronates via Rh(I)CI-catalyzed sequential regioselective hydroboration of 1-alkynes
Endo, Kohei,Hirokami, Munenao,Shibata, Takanori
experimental part, p. 1331 - 1335 (2009/10/23)
A Rh(I)Cl-DPPB-complex-catalyzed sequential hydroboration of aryl alkynes and aliphatic alkynes was achieved. The reaction proceeded with almost perfect regioselectivity to afford 1,1-organodiboronate compounds in moderate to good yield. Georg Thieme Verl
