80394-97-4 Usage
Uses
Used in Pharmaceutical Research and Development:
Ethanone, 1-[6-(1-methylethyl)-3-pyridinyl](9CI) is used as a research compound for its potential therapeutic properties. Its unique structure and the presence of a 1-methylethyl substituent make it an interesting target for the development of novel drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethanone, 1-[6-(1-methylethyl)-3-pyridinyl](9CI) is utilized as a starting point for the design and synthesis of new pharmaceutical agents. Its structural features provide a foundation for exploring various modifications and improvements to enhance its therapeutic potential.
Used in Drug Design and Synthesis:
Ethanone, 1-[6-(1-methylethyl)-3-pyridinyl](9CI) serves as a key component in the drug design and synthesis process. Its unique properties and structural characteristics allow researchers to explore its potential as a precursor for the development of new pharmaceutical compounds with improved efficacy and safety profiles.
Used in Biological and Pharmacological Studies:
Ethanone, 1-[6-(1-methylethyl)-3-pyridinyl](9CI) is employed in biological and pharmacological studies to investigate its specific properties and potential applications. These studies aim to uncover its mechanism of action, target receptors, and therapeutic effects, providing valuable insights for its further development as a pharmaceutical agent.
Check Digit Verification of cas no
The CAS Registry Mumber 80394-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,9 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80394-97:
(7*8)+(6*0)+(5*3)+(4*9)+(3*4)+(2*9)+(1*7)=144
144 % 10 = 4
So 80394-97-4 is a valid CAS Registry Number.
80394-97-4Relevant academic research and scientific papers
Unprotected Amino Acids as Stable Radical Precursors for Heterocycle C-H Functionalization
Mai, Duy N.,Baxter, Ryan D.
supporting information, p. 3738 - 3741 (2016/08/16)
An efficient and general method for the C-H alkylation of heteroarenes using unprotected amino acids as stable alkyl radical precursors is reported. This one-pot procedure is performed open to air under aqueous conditions and is effective for several natural and unnatural amino acids. Heterocycles of varying structure are suitably functionalized, and reactivity trends reflect the nucleophilic character of the radical species generated.
