876-95-9 Usage
Uses
Used in Medicinal Chemistry:
7-Chlorocinnolin-4(1H)-one is used as a pharmaceutical compound for its anti-inflammatory properties, helping to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Antimicrobial Applications:
7-Chlorocinnolin-4(1H)-one is used as an antimicrobial agent, exhibiting activity against various microorganisms, including bacteria and fungi. This makes it a potential candidate for the development of new antibiotics and antifungal drugs.
Used in Antitumor Applications:
7-Chlorocinnolin-4(1H)-one is used as an anti-tumor agent, showing potential in inhibiting the growth and proliferation of cancer cells. Its anti-tumor properties make it a promising candidate for the development of new cancer therapies.
Used in Pharmaceutical Synthesis:
7-Chlorocinnolin-4(1H)-one is used as a building block in the synthesis of pharmaceutical compounds, contributing to the development of new drugs with improved efficacy and reduced side effects. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 876-95-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 876-95:
(5*8)+(4*7)+(3*6)+(2*9)+(1*5)=109
109 % 10 = 9
So 876-95-9 is a valid CAS Registry Number.
876-95-9Relevant academic research and scientific papers
Synthesis, structures and biological activity of some 4-amino-3-cinnoline-carboxylic acid derivatives. Part 2
Stanczak,Lewgowd,Ochocki,Pakulska,Szadowska
, p. 91 - 97 (2007/10/03)
6,7,8-Substituted 4-amino-3-cinnolinecarboxylic acids 1 were condensed with amines to the corresponding 4-amino-3-cinnolinecarboxamides 7, 8. A variety of pharmacological tests showed a significant CNS activity of some new amides. Decarboxylation of 4-amino-3-cinnolinecarboxylic acids 1 yielded the corresponding 4-aminocinnolines 4 and alkaline hydrolysis of 1 gave 4-oxo-3-cinnolinecarboxylic acids 2. The acids 1 were converted into pyrimido[5,4-c]cinnolines 6 on two ways of synthesis.
