Name | 2,4-Dihydroxypyridine |
Synonyms | NSC 37839 NSC 119859 3-Deazauracil 2,4-Pyridinediol Pyridine-2,4-diol 4-Hydroxy-2-pyridone 2,4-Dihydroxypyridine 2(1H)-Pyridone, 4-hydroxy. 2-hydroxypyridin-4(1H)-one 2-Hydroxy-1H-pyridin-4-one 2-hydroxy-3-nitropyridin-4(1H)-one 3-Deazauracil, 4-Hydroxy-2-pyridone, 2,4-PYridinediol 2,4-Pyridinediol, 3-Deazauracil, 4-Hydroxy-2-pyridone |
CAS | 626-03-9 84719-31-3 |
EINECS | 210-924-8 |
InChI | InChI=1/C5H4N2O4/c8-3-1-2-6-5(9)4(3)7(10)11/h1-2H,(H2,6,8,9) |
Molecular Formula | C5H5NO2 |
Molar Mass | 111.1 |
Density | 1.3113 (rough estimate) |
Melting Point | 272-276 °C (lit.) |
Boling Point | 208.19°C (rough estimate) |
Flash Point | 110.6°C |
Water Solubility | 6.211g/L(20 ºC) |
Solubility | DMSO, Methanol |
Vapor Presure | 0.00192mmHg at 25°C |
Appearance | White crystal |
Color | light yellow |
BRN | 108533 |
pKa | pK1:1.37(+1);pK2:6.45(0);pK3:13(+1) (20°C) |
Storage Condition | Inert atmosphere,Room Temperature |
Refractive Index | 1.4260 (estimate) |
MDL | MFCD00006273 |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
RTECS | UV1146800 |
HS Code | 29339900 |
Hazard Class | IRRITANT |
Introduction | 2, 4-dihydroxypyridine (Pyridine-2,4-diol) is a common intermediate in organic synthesis, the appearance was pale yellow powder at normal temperature and pressure. |
Use | 2, 4-dihydroxypyridine as a common intermediate in organic synthesis, the main purpose is to use it as a molecular skeleton for structural modification and synthesis of drug molecules. The hydroxyl group on the molecular structure has a certain acidity, which can be easily made into alkyl ether to protect it, it provides a guarantee for the subsequent conversion of the amide bond. 2, 4-dihydroxypyridine may also be involved in the synthesis of nitrogen-containing heterocyclic ligands as a modified pyridine ring. |