30081-63-1 Usage
Uses
Used in Pharmaceutical and Medicinal Chemistry:
BENZO[F]ISOQUINOLIN-4(3H)-ONE is used as a key building block for the synthesis of complex organic molecules due to its unique molecular structure, contributing to the development of new pharmaceuticals and medicines.
Used in Enzyme Inhibition:
BIQ is utilized as an enzyme inhibitor, playing a role in modulating biological processes by interacting with specific enzymes, which can be beneficial in treating certain diseases.
Used in Anticancer Research:
BENZO[F]ISOQUINOLIN-4(3H)-ONE is employed as a potential anticancer agent, being studied for its ability to target and inhibit the growth of cancer cells, offering a novel approach to cancer treatment.
Used in Neurological Disorder Treatment:
BIQ is used as a therapeutic agent in the treatment of neurological disorders, leveraging its biological activities to potentially alleviate symptoms or slow disease progression.
Used in Biological Imaging:
As a fluorescence probe, BENZO[F]ISOQUINOLIN-4(3H)-ONE is used in biological imaging to visualize and study cellular and molecular processes, aiding in research and diagnostics.
Check Digit Verification of cas no
The CAS Registry Mumber 30081-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,8 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30081-63:
(7*3)+(6*0)+(5*0)+(4*8)+(3*1)+(2*6)+(1*3)=71
71 % 10 = 1
So 30081-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO/c15-13-12-6-5-9-3-1-2-4-10(9)11(12)7-8-14-13/h1-8H,(H,14,15)
30081-63-1Relevant academic research and scientific papers
Synthesis of Isoquinolones by Sequential Suzuki Coupling of 2-Halobenzonitriles with Vinyl Boronate Followed by Cyclization
Jaime-Figueroa, Saul,Bond, Michael J.,Vergara, J. Ignacio,Swartzel, Jake C.,Crews, Craig M.
, p. 8479 - 8488 (2021/06/28)
A novel, facile, and expeditious two-step synthesis of 3,4-unsubstituted isoquinolin-1(2H)-ones from a Suzuki cross-coupling between 2-halobenzonitriles and commercially available vinyl boronates followed by platinum-catalyzed nitrile hydrolysis and cyclization is described.