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5-BROMO-3-METHOXY-2-NITROPYRIDINE

5-BROMO-3-METHOXY-2-NITROPYRIDINE Suppliers list
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Products Intro: Product Name:5-Bromo-3-methoxy-2-nitropyridine
CAS:152684-26-9
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-27108
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Products Intro: Product Name:5-BROMO-3-METHOXY-2-NITROPYRIDINE
CAS:152684-26-9
Purity:98% Package:1KG;3USD
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Products Intro: Product Name:5-bromo-3-methoxy-2-nitropyridine
CAS:152684-26-9
Purity:98% Package:1g;1USD|10g;USD|100g;1USD|1Kg/Bag;1USD|25Kg/Drum;1USD
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
Tel: +8613580539051
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Products Intro: Product Name:5-bromo-3-methoxy-2-nitro-pyridine
CAS:152684-26-9
Purity:0.97 Package:1KG;25KG
Company Name: ANHUI WITOP BIOTECH CO., LTD
Tel: +8615255079626
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Products Intro: Product Name:5-Bromo-3-methoxy-2-nitropyridine
CAS:152684-26-9

5-BROMO-3-METHOXY-2-NITROPYRIDINE manufacturers

5-BROMO-3-METHOXY-2-NITROPYRIDINE Basic information
Product Name:5-BROMO-3-METHOXY-2-NITROPYRIDINE
Synonyms:5-BROMO-3-METHOXY-2-NITROPYRIDINE;3-Bromo-5-methoxy-6-nitropyridine;Pyridine, 5-bromo-3-methoxy-2-nitro-;102903;5-BROMO-3-METHOXY-2-NITROPYRIDINE ISO 9001:2015 REACH
CAS:152684-26-9
MF:C6H5BrN2O3
MW:233.02
EINECS:
Product Categories:Pyridine
Mol File:152684-26-9.mol
5-BROMO-3-METHOXY-2-NITROPYRIDINE Structure
5-BROMO-3-METHOXY-2-NITROPYRIDINE Chemical Properties
Melting point 112℃
Boiling point 335℃
density 1.730
Fp 156℃
storage temp. Inert atmosphere,Room Temperature
pka-8.84±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
Risk Statements 36/37/38
Safety Statements 26
MSDS Information
5-BROMO-3-METHOXY-2-NITROPYRIDINE Usage And Synthesis
Synthesis
3-Bromo-5-methoxypyridine

50720-12-2

5-BROMO-3-METHOXY-2-NITROPYRIDINE

152684-26-9

General procedure for the synthesis of 5-bromo-3-methoxy-2-nitropyridine from 3-bromo-5-methoxypyridine: 3-bromo-5-methoxypyridine (20.91 g, 0.11 mol) was dissolved in concentrated sulphuric acid (63 ml), and nitric acid (5.2 ml, 0.12 mol) was slowly added dropwise in an ice-bath under cooled conditions, and the reaction mixture was stirred for 20 h at room temperature. After completion of the reaction, the mixture was carefully poured into ice water with continuous stirring. The precipitated solid was collected by filtration and washed with cold water. The resulting solid was dissolved in ethyl acetate and the organic layer was washed sequentially with saturated aqueous sodium bicarbonate and saturated brine, followed by drying with anhydrous magnesium sulfate. After filtration to remove the drying agent, the filtrate was concentrated under reduced pressure to afford the target product 5-bromo-3-methoxy-2-nitropyridine (21.97 g, 85% yield) in the form of a light yellow solid. The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz): δ 4.01 (3H, s), 7.68 (1H, d, J = 1.6 Hz), 8.16 (1H, d, J = 1.9 Hz).

References[1] Patent: US2006/84665, 2006, A1. Location in patent: Page/Page column 70
[2] Patent: WO2010/100127, 2010, A1. Location in patent: Page/Page column 69-70
[3] Acta Chemica Scandinavica, 1993, vol. 47, # 8, p. 805 - 812
[4] Recueil des Travaux Chimiques des Pays-Bas, 1955, vol. 74, p. 1171,1174
5-BROMO-3-METHOXY-2-NITROPYRIDINE Preparation Products And Raw materials
Raw materials3,5-Dibromopyridine-->3-Bromo-5-methoxypyridine-->Sulfuric acid-->Nitric acid
Tag:5-BROMO-3-METHOXY-2-NITROPYRIDINE(152684-26-9) Related Product Information
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