CAS 40263-57-8
:2-Iodo-3-pyridinol
Description:
2-Iodo-3-pyridinol is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of an iodine atom at the 2-position and a hydroxyl group (-OH) at the 3-position of the pyridine ring defines its structure and reactivity. This compound typically appears as a solid or crystalline substance and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The iodine substituent can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 2-Iodo-3-pyridinol may participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Its properties, including solubility and stability, can vary depending on the solvent and environmental conditions. As with many halogenated compounds, safety precautions should be observed when handling 2-Iodo-3-pyridinol due to potential toxicity and environmental impact.
Formula:C5H4INO
InChI:InChI=1S/C5H4INO/c6-5-4(8)2-1-3-7-5/h1-3,8H
InChI key:InChIKey=HJBGMPCMSWJZNH-UHFFFAOYSA-N
SMILES:OC1=C(I)N=CC=C1
Synonyms:- 2-Hydroxy-3-Iodopyridine
- 2-Iodo-3-hydroxypyridine
- 2-Iodopyridin-3-Ol
- 3-Hydroxy-2-iodopyridine
- 3-Pyridinol, 2-iodo-
- NSC 103161
- Pyridine, 2-iodo-3-hydroxy-
- 2-Iodo-3-pyridinol
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Found 5 products.
3-Hydroxy-2-iodopyridine
CAS:Formula:C5H4INOPurity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:221.003-Hydroxy-2-iodopyridine
CAS:<p>3-Hydroxy-2-iodopyridine</p>Formula:C5H4INOPurity:95%Color and Shape: light brown to brown solidMolecular weight:221.00g/mol3-Hydroxy-2-iodopyridine
CAS:Formula:C5H4INOPurity:97%Color and Shape:Solid, Yellow powderMolecular weight:220.9972-lodo-3-hydroxypyridine
CAS:<p>2-lodo-3-hydroxypyridine is a chemical compound that is used as a solvent and as a reagent in organic synthesis. 2-Lodo-3-hydroxypyridine has shown potent inhibition against influenza A and B viruses, which are the causative agents of the flu. It also has prognostic value in patients with chronic hepatitis B virus infection. The structure of 2-lodo-3-hydroxypyridine is similar to that of the nucleoside ribonucleotide, which can be synthesized by reacting with compounds such as magnesium ion, phenolate ion, and hydroxylamine. This reaction is known to occur through an electrophilic substitution mechanism, in which the nucleophile attacks the electrophilic carbocation intermediate to form a covalent bond. The optical properties of 2-lodo-3-hydroxypyridine were found by this research group to be sensitive to its environment; they found that when</p>Formula:C5H4INOPurity:Min. 95%Molecular weight:221 g/mol




