189254-22-6 Usage
Description
Ethanone, 1-(9-amino-1-hydroxy-2-acridinyl)-2-(methylsulfinyl)-, is a complex chemical compound characterized by the presence of acridine and sulfinyl groups. The acridine group endows the molecule with fluorescent properties, which can be advantageous for applications in biological imaging and staining. The incorporation of a sulfinyl group introduces a sulfur atom, enhancing the compound's reactivity and potentially broadening its pharmacological applications. This versatile molecule holds promise across various fields, including medicinal chemistry, materials science, and bioimaging.
Uses
Used in Medicinal Chemistry:
Ethanone, 1-(9-amino-1-hydroxy-2-acridinyl)-2-(methylsulfinyl)-, is utilized as a pharmaceutical intermediate for the development of novel therapeutic agents. Its unique structure allows for the design of drugs with specific targeting and activity profiles, potentially leading to more effective treatments for various diseases.
Used in Materials Science:
In the field of materials science, Ethanone, 1-(9-amino-1-hydroxy-2-acridinyl)-2-(methylsulfinyl)-, is employed as a building block for the synthesis of advanced materials with tailored properties. Ethanone, 1-(9-amino-1-hydroxy-2-acridinyl)-2-(methylsulfinyl)-'s reactivity and structural features can be exploited to create new materials with improved performance in areas such as electronics, sensors, and energy storage.
Used in Bioimaging Applications:
Ethanone, 1-(9-amino-1-hydroxy-2-acridinyl)-2-(methylsulfinyl)-, is used as a fluorescent probe in bioimaging applications. Its acridine-based fluorescence allows for the visualization and tracking of biological processes at the molecular level, providing valuable insights into cellular mechanisms and aiding in the diagnosis and study of diseases.
Used in Chemical Synthesis:
Ethanone, 1-(9-amino-1-hydroxy-2-acridinyl)-2-(methylsulfinyl)-, serves as a key intermediate in the synthesis of various organic compounds. Its unique functional groups enable a range of chemical reactions, facilitating the production of specialized molecules for use in research, pharmaceuticals, and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 189254-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,2,5 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 189254-22:
(8*1)+(7*8)+(6*9)+(5*2)+(4*5)+(3*4)+(2*2)+(1*2)=166
166 % 10 = 6
So 189254-22-6 is a valid CAS Registry Number.
