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2-Amino-6-methoxy-3-nitropyridine

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Products Intro: Product Name:2-Amino-6-methoxy-3-nitropyridine
CAS:73896-36-3
Purity:99% Package:1KG;5.00;USD|10KG;3.00;USD|50KG;2.00;USD
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Products Intro: Product Name:2-Amino-6-methoxy-3-nitropyridine
CAS:73896-36-3
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CAS:73896-36-3
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Products Intro: Product Name:6-Methoxy-3-nitropyridin-2-amine
CAS:73896-36-3
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Products Intro: Product Name:2-Amino-6-methoxy-3-nitropyridine
CAS:73896-36-3
Purity:0.98 Package:1g;5g;25g;201g

2-Amino-6-methoxy-3-nitropyridine manufacturers

2-Amino-6-methoxy-3-nitropyridine Basic information
Product Name:2-Amino-6-methoxy-3-nitropyridine
Synonyms:6-Methoxy-3-nitro-pyridin-2-ylamine;2-Amino-6-methoxy-3-nitropyrid;2-AMINO-3-NITRO-6-METHOXYLPYRIDINE;2-Amino-6-methoxy-3-nitropyridine ,98%;TENA-001;6-METHOXY-3-NITRO-2-PYRIDINYLAMINE;2-PYRIDINAMINE, 6-METHOXY-3-NITRO-;2-AMINO-3-NITRO-6-METHOXY PYRIDINE
CAS:73896-36-3
MF:C6H7N3O3
MW:169.14
EINECS:616-028-7
Product Categories:Pyridine;Pyridine series;Amines;Pyridines;Pyridines derivates
Mol File:73896-36-3.mol
2-Amino-6-methoxy-3-nitropyridine Structure
2-Amino-6-methoxy-3-nitropyridine Chemical Properties
Melting point 171-172°C
Boiling point 338.5±37.0 °C(Predicted)
density 1.400±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form solid
pka0.17±0.50(Predicted)
color Yellow
InChI1S/C6H7N3O3/c1-12-5-3-2-4(9(10)11)6(7)8-5/h2-3H,1H3,(H2,7,8)
InChIKeyRDJILYVRVOTMTQ-UHFFFAOYSA-N
SMILESCOc1ccc(c(N)n1)[N+]([O-])=O
CAS DataBase Reference73896-36-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-36/37/38-43
Safety Statements 26-36/37
WGK Germany 3
HazardClass IRRITANT
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Resp. Sens. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
2-Amino-6-methoxy-3-nitropyridine Usage And Synthesis
Chemical PropertiesYellow solid
Synthesis
Sodium Methoxide

124-41-4

2-Amino-6-chloro-3-nitropyridine

27048-04-0

2-Amino-6-methoxy-3-nitropyridine

73896-36-3

1. 7.78 g (0.144 mol) of sodium methanolate was mixed with 50.0 mL of methanol and the mixture was cooled to 15 °C. 2. 25.0 g (0.144 mol) of 2-amino-6-chloro-3-nitropyridine was slowly added to the above solution while maintaining 15°C. 3. the reaction mixture was heated to 25°-30°C and stirred continuously at this temperature for 4-5 hours. 4. The progress of the reaction was monitored by thin layer chromatography (TLC). 5. Upon completion of the reaction, the reaction mixture was slowly poured into water to precipitate the product. 6. The precipitate was collected by filtration and washed with cold water. 7. After drying, 21.0 g of 2-amino-3-nitro-6-methoxypyridine was obtained in 86.5% yield and 99.0% purity by HPLC. 8. 8. The melting point of the product was 167°-169°C. 9. 9. 1H-NMR (CDCl3) data: δ 3.89 ppm (single peak, 3H, OCH3), 6.14-6.16 ppm (twin peaks, 1H), 8.24-8.27 ppm (twin peaks, 1H), 8.16 ppm (single peak, 2H, -NH2).

References[1] Patent: US2006/80790, 2006, A1. Location in patent: Page/Page column 3
[2] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 19 - 32
[3] Journal of Medicinal Chemistry, 1997, vol. 40, # 12, p. 1808 - 1819
[4] Patent: WO2014/57415, 2014, A2. Location in patent: Page/Page column 47
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