4244-37-5 Usage
Uses
Used in Pharmaceutical Industry:
6-Nitroquinoxaline-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its versatile reactivity allows for the formation of different derivatives, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
6-Nitroquinoxaline-2-carboxylic acid is utilized in the synthesis of agrochemicals, specifically as a building block for the development of new pesticides and other crop protection agents. Its chemical properties enable the creation of effective and targeted agrochemicals to improve crop yield and protect against pests and diseases.
Used in Organic Synthesis:
6-Nitroquinoxaline-2-carboxylic acid serves as a valuable building block in organic synthesis due to its ability to undergo various chemical transformations. This allows chemists to create a wide range of derivatives with diverse applications in different industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Antimicrobial Applications:
6-Nitroquinoxaline-2-carboxylic acid has been studied for its antimicrobial properties, making it a potential candidate for the development of new antimicrobial agents. Its ability to inhibit the growth of bacteria and other microorganisms can contribute to the creation of effective treatments for various infections.
Used in Antifungal Applications:
The antifungal properties of 6-Nitroquinoxaline-2-carboxylic acid have been investigated, and it may be used as a starting material for the development of new antifungal agents. Its potential to combat fungal infections can lead to the creation of treatments for various fungal diseases, improving patient outcomes.
Used in Anti-inflammatory Applications:
6-Nitroquinoxaline-2-carboxylic acid has also been studied for its anti-inflammatory properties, indicating its potential use in the development of new anti-inflammatory drugs. Its ability to reduce inflammation can contribute to the treatment of various inflammatory conditions, providing relief and improving the quality of life for patients.
Check Digit Verification of cas no
The CAS Registry Mumber 4244-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4244-37:
(6*4)+(5*2)+(4*4)+(3*4)+(2*3)+(1*7)=75
75 % 10 = 5
So 4244-37-5 is a valid CAS Registry Number.
4244-37-5Relevant academic research and scientific papers
Design, synthesis and molecular docking studies of new azomethine derivatives as promising anti-inflammatory agents
Desai, Sulaksha R.,Desai, Vidya G.,Pissurlenkar, Raghuvir R.
, (2022/01/24)
Herein, we synthesized a series of Ibuprofen-based 4a-k, quinoxaline-based 9a-f and pyridine-based 13a-h azomethine derivatives and studied their anti-inflammatory potency. The in-silico docking studies of the synthesized compounds 4a-k revealed better af
LABELLED ANALOGUES OF HALOBENZAMIDES AS RADIOPHARMACEUTICALS
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Page/Page column 41, (2008/06/13)
The present invention relates to the use of a compound of formula (I): in which R1 represents a radionuclide, Ar represents an aromatic nucleus, m is an integer varying from 2 to 4, R2 and R3 represent, independently of one another, a hydrogen atom, a (C1
Inhibitors of HIV protease
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, (2008/06/13)
Compounds of formula (I): STR1 wherein: R1 is hydrogen, alkyl, aralkyl, --CORa, --CORb, --CSRa, --CSRb, --SO2 Rb, --CONHRb, --CSNHRb, --CONRb Rb or --CSNRb Rb ; R2 is hydrogen or alkyl; R3 is hydrogen, alkylidene, substituted alkyl, or Rb ; R4 is optionally substituted alkyl, cycloalkyl, or aryl; R5 is Rb O--, Rb Rb N--, Rb HN--, aralkyloxycarbonyloxy or aralkyloxycarbonylamino, or R5 is --(CH2)p --D--(CH2)r --, where D is a single bond, carbonyl, oxygen, sulfur, --NH--, --(CH2 =CH2)-- or --NHCO--; and p and r are each 0 or an integer from 1 to 5; A is --(CH2)m --B--(CH2)n -- where B is a single bond, carbonyl, oxygen, sulfur, --NH--, --(CH2 =CH2)-- or --NHCO--; and m and n are each 0 or an integer from 1 to 5; Ra is alkoxy, aralkyloxy, aryloxy or alkoxycarbonyl; Rb is optionally substituted alkyl, cycloalkyl, heterocyclic, aryl or arylalkenyl; and pharmaceutically acceptable salts and esters thereof and pro-drugs therefor, have the ability to inhibit the activity of HIV protease and may thus be used for the treatment and prophylaxis of AIDS.
