CAS 80791-79-3
:5-Bromo-4-hydroxy-2(1H)-pyridinone
Description:
5-Bromo-4-hydroxy-2(1H)-pyridinone, with the CAS number 80791-79-3, is a heterocyclic organic compound characterized by its pyridinone structure, which includes a bromine substituent and a hydroxyl group. This compound typically exhibits a pale yellow to brownish color and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydroxyl group. It is known for its chelating properties, particularly with metal ions, making it useful in various applications, including analytical chemistry and as a potential therapeutic agent. The presence of the bromine atom enhances its reactivity and may influence its biological activity. Additionally, the compound's structure allows for tautomerism, which can affect its chemical behavior and interactions. Safety data indicates that, like many brominated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, 5-Bromo-4-hydroxy-2(1H)-pyridinone is a compound of interest in both research and industrial applications.
Formula:C5H4BrNO2
InChI:InChI=1S/C5H4BrNO2/c6-3-2-7-5(9)1-4(3)8/h1-2H,(H2,7,8,9)
InChI key:InChIKey=RILZSVFBALMCGA-UHFFFAOYSA-N
SMILES:OC=1C(Br)=CNC(=O)C1
Synonyms:- 5-Bromo-4-hydroxy-2-pyridone
- 5-Bromo-4-hydroxy-2(1H)-pyridinone
- 2(1H)-Pyridinone, 5-bromo-4-hydroxy-
- 2,4-Pyridinediol, 5-bromo-
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50
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90
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95
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100
Found 2 products.
3-Bromopyridine-2,4-diol
CAS:<p>3-Bromopyridine-2,4-diol is a potent inhibitor of leukemias. It is an l1210 leukemia cell line, which is sensitive to this drug. 3-Bromopyridine-2,4-diol has been shown to inhibit the proliferation of murine leukemia cells and human leukemia cells that are resistant to other drugs. 3-Bromopyridine-2,4-diol inhibits the growth of viruses by alkylating their DNA and prevents the replication of carbocyclic nucleosides by binding to them. This drug also inhibits the synthesis of viral RNA and DNA in these cells.</p>Formula:C5H4BrNO2Purity:Min. 95%Molecular weight:189.99 g/mol
