ChemicalBook > CAS DataBase List > 2-Chloro-5-fluoro-3-methoxypyridine

2-Chloro-5-fluoro-3-methoxypyridine

Product Name
2-Chloro-5-fluoro-3-methoxypyridine
CAS No.
1097264-89-5
Chemical Name
2-Chloro-5-fluoro-3-methoxypyridine
Synonyms
2-Chloro-5-fluoro-3-methoxypyridine;Pyridine, 2-chloro-5-fluoro-3-methoxy-
CBNumber
CB23064171
Molecular Formula
C6H5ClFNO
Formula Weight
161.56
MOL File
1097264-89-5.mol
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2-Chloro-5-fluoro-3-methoxypyridine Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to light yellow Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Activate Scientific
Product number
AS147065
Product name
2-Chloro-5-fluoro-3-methoxypyridine
Purity
97%
Packaging
100mg
Price
$225
Updated
2021/12/16
AK Scientific
Product number
6255DN
Product name
2-Chloro-5-fluoro-3-methoxypyridine
Packaging
1g
Price
$762
Updated
2021/12/16
Alichem
Product number
1097264895
Product name
2-Chloro-5-fluoro-3-methoxypyridine
Packaging
250mg
Price
$1078
Updated
2021/12/16
Chemenu
Product number
CM174846
Product name
2-chloro-5-fluoro-3-methoxypyridine
Purity
95%
Packaging
1g
Price
$1169
Updated
2021/12/16
Alichem
Product number
1097264895
Product name
2-Chloro-5-fluoro-3-methoxypyridine
Packaging
1g
Price
$3010.8
Updated
2021/12/16
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2-Chloro-5-fluoro-3-methoxypyridine Chemical Properties,Usage,Production

Synthesis

75711-01-2

1097264-89-5

General procedure for the synthesis of 2-chloro-5-fluoro-3-methoxypyridine from 2-chloro-3-methoxy-5-aminopyridine: To a suspension of 2-chloro-3-methoxy-5-aminopyridine (2.14 g, 13.50 mmol) in 4M aqueous HCl (10.12 mL, 40.50 mmol) under ice-bath cooling conditions was slowly added dropwise sodium nitrite ( 1.02 g, 14.84 mmol) dissolved in water (7 mL) was slowly added dropwise for 5 min. After the dropwise addition, the reaction mixture was stirred vigorously at 5 °C for 30 min. Subsequently, a solution of sodium tetrafluoroborate (2.67 g, 24.29 mmol) dissolved in water (17 mL) was added dropwise to the reaction mixture at 5 °C. Upon completion of the reaction, the resulting thick suspension was collected by filtration, washed sequentially with cold water and a small amount of cold ethanol, and then dried under reduced pressure at 55 °C for 8 hours. The resulting black solid was dissolved in xylene (25 mL) and refluxed for 1 hour. After completion of the reaction, the solvent was removed by evaporation under reduced pressure and the residue was dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate. The organic phase was separated, dried with anhydrous sodium sulfate, filtered and the solvent was removed in vacuum. Finally, the black oily material obtained was purified by silica gel fast chromatography (Biotage SP4 25M, cyclohexane/ethyl acetate 95/5) to afford 2-chloro-5-fluoro-3-methoxypyridine (0.11 g, 0.69 mmol, 5% yield) as a light yellow solid.1H NMR (400 MHz, DMSO-d6) δ (ppm): 8.03 ( d, 1H), 7.70 (dd, 1H), 3.92 (s, 3H).

References

[1] Patent: US2009/22670, 2009, A1. Location in patent: Page/Page column 22-23

2-Chloro-5-fluoro-3-methoxypyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Chloro-5-fluoro-3-methoxypyridine Suppliers

Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
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Career Henan Chemica Co
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1097264-89-5, 2-Chloro-5-fluoro-3-methoxypyridineRelated Search:


  • 2-Chloro-5-fluoro-3-methoxypyridine
  • Pyridine, 2-chloro-5-fluoro-3-methoxy-
  • 1097264-89-5