5-Chloro-2-hydroxy-3-nitropyridine
5-Chloro-2-hydroxy-3-nitropyridine Basic information
- Product Name:
- 5-Chloro-2-hydroxy-3-nitropyridine
- Synonyms:
-
- 5-CHLORO-2-HYDROXY-3-NITROPYRIDINE
- 5-CHLORO-3-NITROPYRIDIN-2-OL
- 5-CHLORO-3-NITRO-2-PYRIDINOL
- 2-hydroxy-3-nitro-5-chloropyridine
- 5-Chloro-3-nitropyridin-2-ol, 95+%
- 5-Chloro-2-hydroxy-3-nitropyridine 95+%
- 5-Chloro-2-hydroxy-3-nitropyridine ,97%
- 2-Hydroxy-5-chloro-3-nitropyridine
- CAS:
- 21427-61-2
- MF:
- C5H3ClN2O3
- MW:
- 174.54
- EINECS:
- 622-609-6
- Product Categories:
-
- Heterocycle-Pyridine series
- Chloropyridines
- Halopyridines
- Bases & Related Reagents
- Nucleotides
- blocks
- NitroCompounds
- Pyridines
- Pyridine
- Mol File:
- 21427-61-2.mol
5-Chloro-2-hydroxy-3-nitropyridine Chemical Properties
- Melting point:
- 232-236 °C
- Boiling point:
- 284.1±40.0 °C(Predicted)
- Density
- 1.61±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- soluble in Dimethylformamide
- form
- powder to crystal
- pka
- 6.31±0.10(Predicted)
- color
- Light yellow to Yellow to Green
- BRN
- 383852
- CAS DataBase Reference
- 21427-61-2(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-41-37/38-22
- Safety Statements
- 26-36/37/39-39-36-37
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29337900
MSDS
- Language:English Provider:ALFA
5-Chloro-2-hydroxy-3-nitropyridine Usage And Synthesis
Chemical Properties
White to light brown solid
Uses
5-Chloro-2-hydroxy-3-nitropyridine (cas# 21427-61-2) is a compound useful in organic synthesis.
Synthesis
1072-98-6
21427-61-2
Preparation of Example A2 5-chloro-2-hydroxy-3-nitropyridine (STR9): 321 g of 2-amino-5-chloropyridine was slowly added dropwise to 1.25 L of concentrated sulfuric acid with continuous stirring until the raw material was completely dissolved. Subsequently, 172.5 g of sodium nitrite (dissolved in 240 mL of water) was slowly added at 40°C to 45°C and the reaction mixture continued to be stirred for 15 minutes. Next, 125 mL of pure nitric acid was slowly added dropwise over 40 minutes at 50°C. The reaction mixture was maintained at 55°C for 1 hour and then the reaction was quenched by pouring into 5 kg of ice water. The yellow precipitated product was collected by filtration, washed thoroughly with deionized water and dried at 60°C to afford 351 g of 5-chloro-2-hydroxy-3-nitropyridine in 80.5% of the theoretical yield and a melting point of 229°C to 231°C.
References
[1] Patent: US5274100, 1993, A
[2] Yakugaku Zasshi, 1952, vol. 72, p. 431
[3] Chem.Abstr., 1953, p. 6404
5-Chloro-2-hydroxy-3-nitropyridine Preparation Products And Raw materials
Raw materials
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5-Chloro-2-hydroxy-3-nitropyridine(21427-61-2)Related Product Information
- 4-Hydroxy-3-nitropyridine
- 3-Nitropyridine
- Clopidol
- 3-Nitro-2-pyridinol
- Pentachloropyridine
- 2-Bromo-5-nitropyridine
- 3-Hydroxypyridine
- CHLOROPHOSPHONAZO III
- 2-Chloro-3-hydroxypyridine
- 5-CHLORO-3-PYRIDINAMINE
- 2-HYDROXY-3-NITROPYRIDINE
- 3-CHLORO-5-NITROPYRIDINE
- 5-Chloro-2-ethoxy-3-nitropyridine
- 5-CHLORO-2-HYDROXYPYRIDINE
- 5-Chloro-2-methoxy-3-nitropyridine
- 2-Nitrochlorobenzene
- Difluorochloromethane
- 4-Nitrobenzyl chloride