| Identification | More | [Name]
4-Chloro-2-hydroxy-3-nitropyridine | [CAS]
165547-79-5 | [Synonyms]
4-CHLORO-3-NITRO-2-PYRIDONE
4-CHLORO-3-NITROPYRIDONE
4-Chloro-2-hydroxy-3-nitropyridine
4-Chloro-3-nitro-2-hydroxypyridine
2--3--4-
4-Chloro-3-nitropyridin-2-ol
2-HYDROXY-3-NITRO-4-CHLOROPYRIDINE
4-Chloro-3-nitro-1H-pyridin-2-one | [EINECS(EC#)]
-0 | [Molecular Formula]
C5H3ClN2O3 | [MDL Number]
MFCD03093067 | [Molecular Weight]
174.54 | [MOL File]
165547-79-5.mol |
| Chemical Properties | Back Directory | [Melting point ]
222-224°C | [Boiling point ]
283.4±40.0 °C(Predicted) | [density ]
1.61±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [form ]
solid | [pka]
6.89±0.10(Predicted) | [color ]
Yellow | [Water Solubility ]
Insoluble in water. | [BRN ]
149557 | [InChI]
InChI=1S/C5H3ClN2O3/c6-3-1-2-7-5(9)4(3)8(10)11/h1-2H,(H,7,9) | [InChIKey]
UKIZCTHOMJXNIX-UHFFFAOYSA-N | [SMILES]
C1(=O)NC=CC(Cl)=C1[N+]([O-])=O | [CAS DataBase Reference]
165547-79-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [HS Code ]
2933399990 |
| Hazard Information | Back Directory | [Uses]
4-Chloro-3-nitro-2-pyridone finds an important application as raw material in organic synthesis and pharmaceuticals. It is also used as an intermediate in agrochemicals and dyestuffs. | [Synthesis]
General procedure for the synthesis of 2-hydroxy-3-nitro-4-chloropyridine from 4-hydroxy-3-nitropyridin-2(1H)-one: to 2,4-dihydroxy-3-nitropyridine (5.00 g, 0.032 mol), dimethyl chloride (4.07 g, 0.032 mol), and 5 drops of DMF were added to 2,4-dihydroxy-3-nitropyridine (5.00 g, 0.032 mol) and slowly added dropwise to dichloromethane (80 mL) at 0°C. . The reaction mixture was stirred at room temperature for 4 hours. After the reaction was complete, it was diluted by adding dichloromethane (100 mL). The organic layer was washed sequentially with saturated sodium bicarbonate solution, water and saturated saline. The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target product 2-hydroxy-3-nitro-4-chloropyridine (5.00 g, 89% yield). | [References]
[1] Organic Process Research and Development, 2013, vol. 17, # 12, p. 1561 - 1567
[2] Patent: CN108498516, 2018, A. Location in patent: Paragraph 0023; 0025; 0026; 0027; 0028
[3] Patent: WO2017/14323, 2017, A1. Location in patent: Paragraph 0250
[4] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 15, p. 4986 - 4989
[5] Patent: US2012/289497, 2012, A1. Location in patent: Page/Page column 29 |
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