868944-73-4 Usage
Uses
Used in Organic Synthesis:
3-Cyano-4-(5,5-Dimethyl-[1,3,2]Dioxaborinan-2-Yl)-Pyridine is used as a building block for the synthesis of various organic compounds due to its unique structural features and reactivity.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 3-Cyano-4-(5,5-Dimethyl-[1,3,2]Dioxaborinan-2-Yl)-Pyridine is used as a key intermediate for the development of new drugs and bioactive molecules, contributing to the advancement of medicinal chemistry.
Used in Formation of Carbon-Carbon and Carbon-Heteroatom Bonds:
3-Cyano-4-(5,5-Dimethyl-[1,3,2]Dioxaborinan-2-Yl)-Pyridine is utilized as a reagent in organic reactions for the formation of carbon-carbon and carbon-heteroatom bonds, which are crucial for creating complex molecular structures.
Used in Materials Science:
3-Cyano-4-(5,5-Dimethyl-[1,3,2]Dioxaborinan-2-Yl)-Pyridine has potential applications in materials science, where its unique structural features and reactivity can be harnessed to develop new materials with specific properties.
Used in Catalysis:
In the field of catalysis, 3-Cyano-4-(5,5-Dimethyl-[1,3,2]Dioxaborinan-2-Yl)-Pyridine can be employed as a catalyst or a catalyst precursor to facilitate various chemical reactions, enhancing the efficiency and selectivity of processes in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 868944-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,9,4 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 868944-73:
(8*8)+(7*6)+(6*8)+(5*9)+(4*4)+(3*4)+(2*7)+(1*3)=244
244 % 10 = 4
So 868944-73-4 is a valid CAS Registry Number.
868944-73-4Relevant academic research and scientific papers
Synthesis of azaphenanthridines via anionic ring closure
Hansen, Henriette M.,Lysén, Morten,Begtrup, Mikael,Kristensen, Jesper L.
, p. 9955 - 9960 (2007/10/03)
A new and convergent synthesis of azaphenanthridines via an anionic ring closure is reported. Ortho-lithiation/in situ borylation of cyanopyridines produces the corresponding cyanopyridylboronic esters, which undergo a Suzuki-Miyaura cross-coupling to giv
