723-89-7 Usage
Description
1-Phenylisatin is an organic compound that serves as a versatile reactant in the synthesis of various pharmaceutical agents. It possesses unique chemical properties that make it a valuable component in the development of potential treatments for a range of medical conditions.
Uses
Used in Pharmaceutical Industry:
1-Phenylisatin is used as a reactant for the preparation of indolin-2,3-dione Schiff bases, which have potential applications as antimycobacterial agents. These agents are crucial in the development of treatments for tuberculosis and other mycobacterial infections.
1-Phenylisatin is also used as a reactant for the synthesis of antipyretic agents, which are essential in managing fever and reducing body temperature in cases of infection or inflammation.
In addition, 1-Phenylisatin plays a role in the production of antiproliferative agents, which are compounds that inhibit cell growth and can be used in the treatment of cancer and other hyperproliferative disorders.
Furthermore, 1-Phenylisatin is utilized in the creation of phenylacetamides, which have anticonvulsant properties. These agents are vital in the management of epilepsy and other seizure disorders.
Lastly, 1-Phenylisatin is used in the development of selective Galanin GAL3 receptor antagonists. These antagonists have potential therapeutic applications in the treatment of various neurological and psychiatric conditions, such as depression, anxiety, and pain management.
Check Digit Verification of cas no
The CAS Registry Mumber 723-89-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 723-89:
(5*7)+(4*2)+(3*3)+(2*8)+(1*9)=77
77 % 10 = 7
So 723-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H9NO2/c16-13-11-8-4-5-9-12(11)15(14(13)17)10-6-2-1-3-7-10/h1-9H
723-89-7Relevant articles and documents
PROTECTIVE EFFECTS OF ISATINS IN HYPOBARIC HYPOXIA
Stankyavichyus, A. P.,Mazhilis, L. I.,Garalene, V. N.,Risyalis, S. P.,Sapragonene, M. S.,Dzhyakcheryus, L. M.
, p. 858 - 861 (1981)
-
One-pot method for preparing 9 - acridine formic acid
-
Paragraph 0018-0051, (2021/11/10)
The invention discloses a one-pot method for preparing 9 - acridine formic acid. After completion of the reaction, the unreacted oxalyl chloride and the reaction solvent are then distilled 5 - 10 °C off under reduced pressure until the reaction is complet
Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo- and Enantioconvergent Michael–Henry Reactions to Afford Spirooxindoles Bearing Furan-Fused Rings
Sohail, Muhammad,Tanaka, Fujie
supporting information, p. 21256 - 21260 (2021/08/23)
Dynamic kinetic asymmetric transformation (DYKAT) reactions of racemic diastereomer mixtures that afford the products as essentially single diastereomers with high enantioselectivities are described. We demonstrated the DYKAT in the diastereo- and enantio
