911461-03-5 Usage
Description
4-Hydroxy-5-nitropyridine-3-carboxylic acid is a chemical compound with the molecular formula C6H4N2O5. It is a derivative of pyridine, featuring a hydroxyl group at the 4-position, a nitro group at the 5-position, and a carboxylic acid group at the 3-position. 4-Hydroxy-5-nitropyridine-3-carboxylic acid is commonly used as a building block in the synthesis of pharmaceuticals and organic chemicals due to its versatile reactivity and functional groups. Additionally, it exhibits potential biological activity, making it a target for drug discovery and development. 4-Hydroxy-5-nitropyridine-3-carboxylic acid is a yellow solid at room temperature and is sparingly soluble in water. It is important to handle this compound with caution, as it may present hazards if not properly handled and stored.
Uses
Used in Pharmaceutical Industry:
4-Hydroxy-5-nitropyridine-3-carboxylic acid is used as a building block for the synthesis of pharmaceuticals and organic chemicals. Its versatile reactivity and functional groups make it a valuable component in the development of new drugs and therapeutic agents.
Used in Drug Discovery and Development:
4-Hydroxy-5-nitropyridine-3-carboxylic acid is used as a target for drug discovery and development due to its potential biological activity. Researchers are interested in exploring its properties and applications in creating new medications and treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 911461-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,4,6 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 911461-03:
(8*9)+(7*1)+(6*1)+(5*4)+(4*6)+(3*1)+(2*0)+(1*3)=135
135 % 10 = 5
So 911461-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N2O5/c9-5-3(6(10)11)1-7-2-4(5)8(12)13/h1-2H,(H,7,9)(H,10,11)
911461-03-5Relevant articles and documents
Novel tricyclic poly (ADP-ribose) polymerase-1/2 inhibitors with potent anticancer chemopotentiating activity: Design, synthesis and biological evaluation
Li, Hui,Hu, Yan,Wang, Xueyan,He, Guangwei,Xu, Yungen,Zhu, Qihua
, p. 4731 - 4740 (2016)
8,9-Dihydro-2,4,7,9a-tetraazabenzo[cd]azulen-6(7H)-ones were designed and synthesized as a new class of PARP-1/2 inhibitors. The compounds displayed a variable pattern of PARP-1/2 enzymes inhibition profile that, in part, paralleled the antiproliferative
Transformations of ortho-methoxyaryl(hetaryl)carboxamides into quinazolin-4-one and pyrido[2,3-d]pyrimidin-4-one derivatives
Ryabova,Makarov,Alekseeva,Shashhov,Chernyshev,Granik
, p. 1907 - 1914 (2007/10/03)
ortho-Chloroaryl(hetaryl)carboxamides containing one or two nitro groups at positions 3 and/or 5 of the ring undergo condensation accompanied by the pyrimidine ring closure on refluxing in an excess of sodium methoxide to form bicyclic products, viz., qui
