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5-Bromo-2,3-dimethoxypyridine

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:5-Bromo-2,3-dimethoxypyridine
CAS:52605-98-8
Purity:97% Min. Package:1G;1KG;100KG
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Products Intro: Product Name:5-Bromo-2,3-dimethoxypyridine
CAS:52605-98-8
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-57698
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Products Intro: Product Name:5-Bromo-2,3-dimethoxypyridine
CAS:52605-98-8
Purity:99% Package:1KG;9.20USD
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Products Intro: Product Name:5-Bromo-2,3-dimethoxypyridine
CAS:52605-98-8
Purity:0.98 Package:100g;500g;1kg;5kg;25kg Remarks:customized
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Products Intro: Product Name:5-Bromo-2,3-dimethoxypyridine
CAS:52605-98-8

5-Bromo-2,3-dimethoxypyridine manufacturers

5-Bromo-2,3-dimethoxypyridine Basic information
Product Name:5-Bromo-2,3-dimethoxypyridine
Synonyms:5-Bromo-2,3-dimethoxypyridine;Pyridine, 5-bromo-2,3-dimethoxy-;5-Bromo-2,3-dimethoxypyridine ISO 9001:2015 REACH
CAS:52605-98-8
MF:C7H8BrNO2
MW:218.05
EINECS:
Product Categories:
Mol File:52605-98-8.mol
5-Bromo-2,3-dimethoxypyridine Structure
5-Bromo-2,3-dimethoxypyridine Chemical Properties
Boiling point 222.7±35.0 °C(Predicted)
density 1.484±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
form solid
pka2.19±0.10(Predicted)
AppearanceColorless to off-white <32°C Solid,>32°C Liquid
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HazardClass IRRITANT
MSDS Information
5-Bromo-2,3-dimethoxypyridine Usage And Synthesis
Synthesis
2,5-Dibromo-3-methoxypyridine

1142191-57-8

Sodium Methoxide

124-41-4

5-Bromo-2,3-dimethoxypyridine

52605-98-8

As shown in Step 2-iv of Scheme 2, a methanolic solution of 2,5-dibromo-3-methoxypyridine (13.0 g, 43.8 mmol) and 25 wt% sodium methanolate (95.0 mL, 438.3 mmol) was placed in a reaction vial and the reaction was stirred for 3 hours at 75 °C. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently extracted by adding ethyl acetate and saturated saline. The organic phase was separated, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to afford 5-bromo-2,3-dimethoxypyridine (9.1 g, 95% yield). The product was characterized as follows: ESMS (M + 1) = 218/220; 1H NMR (DMSO-d6) δ 7.8 (d, 1H), 7.46 (d, 1H), 3.81 (s, 3H), 3.86 (s, 3H).

References[1] Patent: US2011/81316, 2011, A1. Location in patent: Page/Page column 14; 15
5-Bromo-2,3-dimethoxypyridine Preparation Products And Raw materials
Raw materials5-BROMO-2-CHLORO-3-METHOXYPYRIDINE-->2,5-Dibromo-3-methoxypyridine-->Sodium Methoxide-->Sodium ethoxide
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