94205-62-6 Usage
Uses
Used in Pharmaceutical Research:
2-(4-AMINO-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID serves as a key compound in pharmaceutical research for its potential therapeutic applications. It is used as a precursor or a building block in the synthesis of new drugs targeting various diseases.
Used in Cancer Research:
In cancer research, 2-(4-AMINO-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID is utilized as a potential anti-cancer agent. It is studied for its ability to interact with biological targets that play a role in cancer development and progression, offering a promising avenue for the discovery of new cancer treatments.
Used in Inflammation Research:
2-(4-AMINO-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID is also used in inflammation research as a potential anti-inflammatory agent. Its properties are being investigated for their capacity to modulate inflammatory responses, which could lead to the development of new treatments for inflammatory diseases.
Used in Chemical Synthesis:
2-(4-AMINO-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID is employed as an intermediate in chemical synthesis, particularly for the production of other quinoline-based compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Material Science:
In material science, 2-(4-AMINO-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID is used in the development of new materials with specific properties, such as光电性能 (photoelectric properties), which can be applied in optoelectronic devices and other advanced technologies.
Used in Agrochemical Research:
2-(4-AMINO-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID is utilized in agrochemical research for its potential applications in the development of new pesticides or herbicides, where its interaction with biological targets can offer novel approaches to pest and weed control.
Each application highlights the versatility and importance of 2-(4-AMINO-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID in various fields, emphasizing its potential to contribute to advancements in medicine, materials, and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 94205-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,0 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94205-62:
(7*9)+(6*4)+(5*2)+(4*0)+(3*5)+(2*6)+(1*2)=126
126 % 10 = 6
So 94205-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H12N2O2/c17-11-7-5-10(6-8-11)15-9-13(16(19)20)12-3-1-2-4-14(12)18-15/h1-9H,17H2,(H,19,20)
94205-62-6Relevant academic research and scientific papers
QUINOLINE COMPOUNDS AS MODULATORS OF RAGE ACTIVITY AND USES THEREOF
-
Paragraph 00363; 00442, (2017/11/15)
Quinoline compounds are disclosed that have a formula represented by the following: and wherein Cy, R1, R4a, R4b, and n are as described herein. The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, diabetes complications, inflammation, and neurodegeneration, obesity, cancer, ischemia/reperfusion injury, cardiovascular disease and other diseases related to RAGE activity.
Energy efficient Pfitzinger reaction: A novel strategy using a surfactant catalyst
More, Priyanka A.,Shankarling, Ganapati S.
supporting information, p. 12380 - 12383 (2017/11/06)
A novel energy efficient method for the Pfitzinger reaction is demonstrated, which is catalysed using a surfactant, cetyltrimethylammonium hydroxide. The surfactant nature of the catalyst caused the substrate to be soluble in aqueous media, which enhanced the interaction of the catalyst with the substrate. An increase in the rate of reaction and more than 78% of energy saving were observed under ultrasonic irradiation.
