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2,6-Dichloro-3-methyl-5-nitropyridine

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Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:58596-88-6
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:2,6-Dichloro-3-methyl-5-nitropyridine
CAS:58596-88-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-24382
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:2,6-dichloro-3-methyl-5-nitropyridine
CAS:58596-88-6
Purity:99% Package:1kg
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
Tel: +8613580539051
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Products Intro: Product Name:2,6-Dichloro-3-methyl-5-nitropyridine
CAS:58596-88-6
Purity:0.97 Package:1KG;25KG
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Tel: +86-0371-86658258 +8613203830695
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Products Intro: Product Name:2,6-Dichloro-3-methyl-5-nitropyridine
CAS:58596-88-6
Purity:98.8%min emma@coreychem.com Package:1KG;2.18USD

2,6-Dichloro-3-methyl-5-nitropyridine manufacturers

2,6-Dichloro-3-methyl-5-nitropyridine Basic information
Product Name:2,6-Dichloro-3-methyl-5-nitropyridine
Synonyms:2,6-Dichloro-3-methyl-5-nitropyridine;Pyridine, 2,6-dichloro-3-Methyl-5-nitro-;2,6-Dichloro-3-methyl-5-nitropyridine ISO 9001:2015 REACH
CAS:58596-88-6
MF:C6H4Cl2N2O2
MW:207.01
EINECS:
Product Categories:
Mol File:58596-88-6.mol
2,6-Dichloro-3-methyl-5-nitropyridine Structure
2,6-Dichloro-3-methyl-5-nitropyridine Chemical Properties
Melting point 70-71 °C(Solv: cyclohexane (110-82-7))
Boiling point 323.5±37.0 °C(Predicted)
density 1.537
storage temp. Inert atmosphere,Room Temperature
pka-5.36±0.10(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
HS Code 2933399990
MSDS Information
2,6-Dichloro-3-methyl-5-nitropyridine Usage And Synthesis
Synthesis
Pyridine, 2-chloro-5-methyl-3-nitro-, 1-oxide

1241373-24-9

2,6-Dichloro-3-methyl-5-nitropyridine

58596-88-6

General procedure for the synthesis of 2,6-dichloro-3-methyl-5-nitropyridine-1-oxide from 2-chloro-5-methyl-3-nitropyridine-1-oxide: 2-chloro-5-methyl-3-nitropyridine-1-oxide (4.0 g, 21.2 mmol) was suspended in phosphorus triclosan (ca. 20 mL) and the reaction was heated to reflux temperature for 3 hours. After completion of the reaction, the reaction mixture was carefully poured into preheated water and cooled to room temperature. It was extracted with ethyl acetate (3×), the organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 4.5 g of brown solid. The crude product was purified by fast column chromatography (dichloromethane as eluent and 5% ethyl acetate in heptane solution as elution system) to give 3.56 g (81% yield) of off-white solid. The product was analyzed by GC-MS (EI+) with m/z = 189 and purity >95%.

References[1] Patent: WO2010/94645, 2010, A1. Location in patent: Page/Page column 26
2,6-Dichloro-3-methyl-5-nitropyridine Preparation Products And Raw materials
Raw materialsPYRIDINE, 2-CHLORO-5-METHYL-, 1-OXIDE-->Pyridine, 2-chloro-5-methyl-3-nitro-, 1-oxide
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