64230-47-3 Usage
Uses
Used in Pharmaceutical Research:
(3-bromo-2-oxo-2,3-dihydro-1H-indol-3-yl)acetic acid is used as a research compound for its potential medicinal properties. (3-bromo-2-oxo-2,3-dihydro-1H-indol-3-yl)acetic acid's structural features make it a valuable candidate for the development of new therapeutic agents.
Used in Anti-inflammatory Applications:
In the field of pharmaceuticals, (3-bromo-2-oxo-2,3-dihydro-1H-indol-3-yl)acetic acid is used as an anti-inflammatory agent due to its potential to alleviate inflammation, which is a common factor in various diseases and conditions.
Used in Analgesic Applications:
(3-bromo-2-oxo-2,3-dihydro-1H-indol-3-yl)acetic acid is also utilized as an analgesic agent, aiming to relieve pain by potentially interacting with pain receptors or pathways in the body.
Used in Anticancer Applications:
Within the oncology sector, (3-bromo-2-oxo-2,3-dihydro-1H-indol-3-yl)acetic acid is used as a potential anticancer agent. It is being studied for its activity against certain types of cancer, with the goal of developing more effective treatments for patients.
Used in Medicinal Chemistry Research:
(3-bromo-2-oxo-2,3-dihydro-1H-indol-3-yl)acetic acid serves as a key compound in medicinal chemistry research, where it is investigated for its potential to be modified or used as a building block for the creation of new drugs with various therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 64230-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64230-47:
(7*6)+(6*4)+(5*2)+(4*3)+(3*0)+(2*4)+(1*7)=103
103 % 10 = 3
So 64230-47-3 is a valid CAS Registry Number.
64230-47-3Relevant academic research and scientific papers
Synthesis of some new spiro[indoline-3,2′-(1′,2′,3′,4′- tetrahydroquinoline)]-2,4′-dione derivatives
Al-Thebeiti, Marzoog S.
, p. 145 - 150 (2007/10/03)
Indole-2,3-dione (1) was treated with malonic acid in a mixture of ethanol/pyridine to afford 3-(2-oxoindolinylidine)acetic acid (2), which then reacted with hydrobromic acid to yield 3-bromo-3-(2-oxoindole)acetic acid (3). Compound (3) reacted with aroma
