741709-61-5 Usage
Uses
Used in Organic Synthesis:
6-Ethyl-3-pyridinyl boronic acid pinacol ester is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in constructing complex organic molecules. Its pinacol ester moiety provides the necessary stability and reactivity for these reactions, making it a preferred choice in organic synthesis.
Used in the Suzuki-Miyaura Coupling Reaction:
In the field of organic chemistry, 6-ethyl-3-pyridinyl boronic acid pinacol ester is utilized as a key component in the Suzuki-Miyaura coupling reaction. This reaction is a significant process in the synthesis of pharmaceuticals, agrochemicals, and materials, allowing for the formation of carbon-carbon bonds between an organoboron compound and an organic halide or triflate.
Used in Medicinal Chemistry and Drug Discovery:
6-Ethyl-3-pyridinyl boronic acid pinacol ester is used as a potential candidate in medicinal chemistry and drug discovery. As a boronic acid derivative, it can interact with biological systems, offering opportunities for the development of new therapeutic agents. Its unique structure and reactivity make it a promising starting point for the design of novel drugs and pharmaceutical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-ethyl-3-pyridinyl boronic acid pinacol ester is used as a building block for the synthesis of various pharmaceutical compounds. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it a valuable asset in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
6-Ethyl-3-pyridinyl boronic acid pinacol ester is also used in the agrochemical industry for the synthesis of agrochemicals. Its role in the Suzuki-Miyaura coupling reaction allows for the creation of new agrochemical compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Materials Science:
In the field of materials science, 6-ethyl-3-pyridinyl boronic acid pinacol ester is used in the synthesis of various materials with unique properties. Its involvement in the formation of carbon-carbon and carbon-heteroatom bonds contributes to the development of advanced materials with potential applications in various industries, such as electronics, energy, and nanotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 741709-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,7,0 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 741709-61:
(8*7)+(7*4)+(6*1)+(5*7)+(4*0)+(3*9)+(2*6)+(1*1)=165
165 % 10 = 5
So 741709-61-5 is a valid CAS Registry Number.