5-Chloro-3-fluoro-2-nitropyridine

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Company Name: Shanxi Xuanran Import and Export Trade Co., Ltd.
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Products Intro: Product Name:5-Chloro-3-fluoro-2-nitropyridine
CAS:1064783-29-4
Purity:0.99 Package:100g;500g;1kg;5kg;25kg Remarks:customized
Company Name: Shanxi Tihondan Pharmaceutical Technology Co., Ltd
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Products Intro: Product Name:5-Chloro-3-fluoro-2-nitropyridine
CAS:1064783-29-4
Purity:95%+ Package:5g;10g;1kg;10kg
Company Name: Aladdin Scientific
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Products Intro: Product Name:5-Chloro-3-fluoro-2-nitropyridine
CAS:1064783-29-4
Purity:98% Package:$81.9/100mg;$167.9/250mg;$601.9/1g;$2704.9/5g;Bulk package Remarks:98%
Company Name: Suzhou ARTK Medchem Co., Ltd.
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Products Intro: Product Name:5-chloro-3-fluoro-2-nitro-pyridine
CAS:1064783-29-4
Purity:0.98 Package:100KG;25KG;10KG;1KG
Company Name: Amadis Chemical Company Limited
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Products Intro: Product Name:5-chloro-3-fluoro-2-nitro-Pyridine
CAS:1064783-29-4
Purity:0.97 Package:mgs,gs,kgs Remarks:A895817
5-Chloro-3-fluoro-2-nitropyridine Basic information
Product Name:5-Chloro-3-fluoro-2-nitropyridine
Synonyms:5-Chloro-3-fluoro-2-nitropyridine;Pyridine, 5-chloro-3-fluoro-2-nitro-
CAS:1064783-29-4
MF:C5H2ClFN2O2
MW:176.53
EINECS:
Product Categories:
Mol File:1064783-29-4.mol
5-Chloro-3-fluoro-2-nitropyridine Structure
5-Chloro-3-fluoro-2-nitropyridine Chemical Properties
Boiling point 266.7±35.0 °C(Predicted)
density 1.595±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka-7.31±0.32(Predicted)
AppearanceOff-white to light brown Solid
Safety Information
MSDS Information
5-Chloro-3-fluoro-2-nitropyridine Usage And Synthesis
Synthesis
2-Amino-5-chloro-3-fluoropyridine

246847-98-3

5-Chloro-3-fluoro-2-nitropyridine

1064783-29-4

Example 4 (b) Synthesis of 5-chloro-3-fluoro-2-nitropyridine: In a 250 mL round-bottom flask, 2-amino-5-chloro-3-fluoropyridine (1.5 g, 1.46 mmol) and concentrated sulfuric acid (50 mL) were added with the stirrer installed. The mixture was stirred until completely dissolved and potassium thiosulfate (13 g, 50 mmol) was added in batches. The reaction mixture was stirred overnight, during which the color gradually changed from light green to dark yellow. After completion of the reaction, the mixture was slowly poured into 500 g of ice and stirring was continued for 10 minutes. Subsequently, solid sodium carbonate was added in batches to adjust the pH to 8-10. the products were extracted with ethyl acetate, the organic phases were combined and concentrated to dryness. The crude product was purified by column chromatography (eluent: 10-15% hexane solution of ethyl acetate) to afford 5-chloro-3-fluoro-2-nitropyridine (0.99 g, 5.6 mmol, 54% yield). The structure of the product was confirmed by 1H NMR (d6-DMSO).

References[1] Patent: US2008/242695, 2008, A1. Location in patent: Page/Page column 34
[2] Patent: US2014/315888, 2014, A1. Location in patent: Paragraph 1071-1072
[3] Patent: WO2017/103824, 2017, A1. Location in patent: Paragraph 00164; 00165
5-Chloro-3-fluoro-2-nitropyridine Preparation Products And Raw materials
Raw materials2-Amino-5-chloro-3-fluoropyridine-->Sulfuric acid-->Potassium thiosulfate
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