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2-AMINO-3-NITRO-5-PICOLINE

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Products Intro: Product Name:2-AMINO-3-NITRO-5-PICOLINE
CAS:7598-26-7
Purity:99.0% Package:1KG;0.1USD
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CAS:7598-26-7
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CAS:7598-26-7
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Products Intro: Product Name:2-AMINO-3-NITRO-5-PICOLINE
CAS:7598-26-7
Purity:95%-99% Package:1kg;1USD

2-AMINO-3-NITRO-5-PICOLINE manufacturers

2-AMINO-3-NITRO-5-PICOLINE Basic information
Product Name:2-AMINO-3-NITRO-5-PICOLINE
Synonyms:2-AMINO-3-NITRO-5-PICOLINE;2-AMINO-5-METHYL-3-NITROPYRIDINE;6-AMINO-5-NITRO-3-PICOLINE;AMINO(2-)-3-NITRO-5-METHYLPYRIDINE;2-Pyridinamine, 5-methyl-3-nitro-;5-Methyl-3-nitropyridin-2-amine;6-Amino-5-nitro-3-picoline, 98+%;5-Methyl-3-nitro-2-aminopyridine
CAS:7598-26-7
MF:C6H7N3O2
MW:153.14
EINECS:690-065-7
Product Categories:amine | nitro-compound;Amino-pyridine series;Amines;Pyridines;Pyridine series;Pyridine;Heterocyclic Compounds;compounds of pyridine
Mol File:7598-26-7.mol
2-AMINO-3-NITRO-5-PICOLINE Structure
2-AMINO-3-NITRO-5-PICOLINE Chemical Properties
Melting point 189-193 °C
Boiling point 318.9±37.0 °C(Predicted)
density 1.354±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka2.54±0.49(Predicted)
form Crystalline Powder
color Ochre
CAS DataBase Reference7598-26-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 36/37/39-26-22
HS Code 29333999
MSDS Information
ProviderLanguage
ACROS English
2-AMINO-3-NITRO-5-PICOLINE Usage And Synthesis
Chemical PropertiesOchre crystalline powder
Synthesis
2-Amino-5-methylpyridine

1603-41-4

2-AMINO-3-NITRO-5-PICOLINE

7598-26-7

Example 170: Synthesis of 5-methyl-3-nitropyridin-2-amine; Sulfuric acid (97%, 100 mL) was placed in a cooling bath at -10°C. When the internal temperature reached 5°C, 2-amino-5-methylpyridine (25 g, 231.2 mmol) was added in batches with stirring (1 hour elapsed time). The suspension was stirred at room temperature until the remaining solid was completely dissolved. The resulting solution was heated to 55 °C and kept 70% conical. Nitric acid (15.6 mL) was added dropwise while maintaining an internal temperature between 55-60 °C. After addition, the mixture was continued to be stirred for 30 minutes and then poured into crushed ice (800 g). The mixture was stirred until completely dissolved and subsequently adjusted to pH 9 with 40% aqueous sodium hydroxide at 0 °C. The reaction mixture was extracted with chloroform (3 x 250 mL). The organic layers were combined, washed with brine (2 x 200 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give 5-methyl-3-nitropyridin-2-amine (9.49 g) as a yellow solid in 27% yield. esms m/z (relative strength): 154 (M + H)+ (100).

References[1] Patent: WO2006/76644, 2006, A2. Location in patent: Page/Page column 204
[2] Journal of Medicinal Chemistry, 1997, vol. 40, # 22, p. 3679 - 3686
[3] Journal of the American Chemical Society, 1951, vol. 73, p. 3504
[4] Journal of the American Chemical Society, 1950, vol. 72, p. 2806
[5] Journal of the American Chemical Society, 1955, vol. 77, p. 3154
2-AMINO-3-NITRO-5-PICOLINE Preparation Products And Raw materials
Raw materialsSodium hydroxide-->Sulfuric acid-->Nitric acid-->2-Amino-5-methylpyridine
Preparation Products2,3-Diamino-5-methylpyridine-->2-BROMO-3-NITRO-5-METHYL PYRIDINE
Tag:2-AMINO-3-NITRO-5-PICOLINE(7598-26-7) Related Product Information
2-Hydrazinyl-5-methyl-3-nitropyridine 2-METHYLAMINO-3-NITRO-5-(TRIFLUOROMETHYL)PYRIDINE 2-AMINO-5-NITRO-6-PICOLINE,2-AMINO-5-NITRO-6-PICOLINE (2-AMINO-6-METHYL-5-NITROPYRIDINE),6-AMINO-3-NITRO-2-PICOLINE 2-AMINO-5-NITRO-4-PICOLINE (2-AMINO-4-METHYL-5-NITROPYRIDINE),2-AMINO-5-NITRO-4-PICOLINE 2-AMINO-3-NITRO-4-PICOLINE,2-AMINO-3-NITRO-4-PICOLINE (2-AMINO-4-METHYL-3-NITROPYRIDINE) 2-AMINO-3-NITRO-5-PICOLINE 3-Nitropyridine 2-Amino-3-nitropyridine 2-Amino-3-nitro-6-picoline 2-Amino-3-methyl-5-nitropyridine methyl 6-amino-5-nitropyridine-3-carboxylate 2-Amino-3-nitro-5-trifluoromethylpyridine 2-HYDRAZINO-3-NITRO-5-(TRIFLUOROMETHYL)PYRIDINE 4-AMINO-3-NITRO-2-PICOLINE BUTTPARK 25\01-33 5-(3,4-dichlorophenyl)-3-nitropyridin-2-amine 6'-METHOXY-5-NITRO-[3,3']BIPYRIDINYL-6-YL-AMINE AURORA KA-6296