868997-86-8 Usage
Uses
Used in Organic Synthesis:
4-(Diisopropylcarbamoyl)pyridin-3-ylboronic acid is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the development of complex organic compounds with potential applications in various fields.
Used in Pharmaceutical Research:
In pharmaceutical research, 4-(Diisopropylcarbamoyl)pyridin-3-ylboronic acid is utilized as a key component in the synthesis of medicinal drugs. Its ability to form carbon-carbon bonds through Suzuki-Miyaura coupling reactions makes it a valuable reagent in the development of new pharmaceutical agents.
Used in Suzuki-Miyaura Coupling Reactions:
4-(Diisopropylcarbamoyl)pyridin-3-ylboronic acid is used as a reagent in Suzuki-Miyaura coupling reactions, which are crucial for forming carbon-carbon bonds. This reaction is widely employed in the synthesis of organic compounds, including those with potential pharmaceutical applications.
Used in Medicinal Drug Development:
4-(Diisopropylcarbamoyl)pyridin-3-ylboronic acid has potential applications in the development of medicinal drugs. Its unique structure and reactivity make it a promising candidate for the creation of new drug molecules with therapeutic properties.
Used in Agrochemical Development:
In the agrochemical industry, 4-(Diisopropylcarbamoyl)pyridin-3-ylboronic acid may be used in the development of new agrochemicals. Its potential applications in this field highlight the versatility of 4-(DiisopropylcarbaMoyl)pyridin-3-ylboronic acid and its importance in various sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 868997-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,9,9 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 868997-86:
(8*8)+(7*6)+(6*8)+(5*9)+(4*9)+(3*7)+(2*8)+(1*6)=278
278 % 10 = 8
So 868997-86-8 is a valid CAS Registry Number.
868997-86-8Relevant academic research and scientific papers
The discovery of tricyclic pyridone JAK2 inhibitors. Part 1: Hit to lead
Siu, Tony,Kozina, Ekaterina S.,Jung, Joon,Rosenstein, Craig,Mathur, Anjili,Altman, Michael D.,Chan, Grace,Xu, Lin,Bachman, Eric,Mo, Jan-Rung,Bouthillette, Melaney,Rush, Thomas,Dinsmore, Christopher J.,Marshall, C. Gary,Young, Jonathan R.
scheme or table, p. 7421 - 7425 (2011/02/23)
This paper describes the discovery and design of a novel class of JAK2 inhibitors. Furthermore, we detail the optimization of a screening hit using ligand binding efficiency and log D. These efforts led to the identification of compound 41, which demonstrates in vivo activity in our study.
