868944-75-6 Usage
Uses
Used in Organic Synthesis:
2-Cyanopyridine-3-boronic acid neopentyl glycol ester is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, such as cross-coupling and Suzuki-Miyaura reactions. Its boronic acid functionality allows it to act as a nucleophile, facilitating the formation of new carbon-carbon or carbon-heteroatom bonds, which is crucial for the synthesis of complex organic molecules and pharmaceutical compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Cyanopyridine-3-boronic acid neopentyl glycol ester can be employed as a building block for the development of novel therapeutic agents. Its structural features can be tailored to target specific biological receptors or enzymes, potentially leading to the discovery of new drugs with improved efficacy and selectivity.
Used in Material Science:
2-Cyanopyridine-3-boronic acid neopentyl glycol ester may also find applications in material science, particularly in the design and synthesis of new polymers, coatings, or adhesives. The cyano and boronic acid groups can impart unique properties to these materials, such as enhanced adhesion, improved thermal stability, or specific binding capabilities.
Used in Analytical Chemistry:
Furthermore, 2-Cyanopyridine-3-boronic acid neopentyl glycol ester can be utilized in analytical chemistry as a derivatizing agent or a chiral selector. Its ability to form stable complexes with various analytes can improve the detection and separation of compounds in chromatographic or spectroscopic techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 868944-75-6 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 868944-75:
(8*8)+(7*6)+(6*8)+(5*9)+(4*4)+(3*4)+(2*7)+(1*5)=246
246 % 10 = 6
So 868944-75-6 is a valid CAS Registry Number.
868944-75-6Relevant 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
