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2,5-DibroMo-4-nitropyridine

2,5-DibroMo-4-nitropyridine Suppliers list
Company Name: Accela ChemBio Inc.
Tel: +1-858-6993322 +86-18019713315
Email: info@accelachem.com
Products Intro: Product Name:2,5-Dibromo-4-nitropyridine
CAS:221241-31-2
Purity:>95% Package:0.1g;0.25g;1g;5g
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
Tel: +8613580539051
Email: joe@yuhengpharm.com
Products Intro: Product Name:2,5-dibromo-4-nitropyridine
CAS:221241-31-2
Purity:0.97 Package:1KG;25KG
Company Name: KARMEL TECHNOLOGY (HK) CO.,LIMITED
Tel: +8618795957998
Email: karmelhk@126.com
Products Intro: Product Name:2,5-DibroMo-4-nitropyridine
CAS:221241-31-2
Purity:0.98 Package:1g; 5g; 10g; 25g; 100g
Company Name: Dideu Industries Group Limited
Tel: +8617392712697
Email: 1022@dideu.com
Products Intro: Product Name:4-[(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthyl)carbonyl]benzoic acid methyl ester
CAS:221241-31-2
Purity:98% Package:25KG Remarks:1097
Company Name: CR Corporation Limited
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Email: fred.wen@crcorporation.cn
Products Intro: Product Name:2,5-DibroMo-4-nitropyridine
CAS:221241-31-2
2,5-DibroMo-4-nitropyridine Basic information
Product Name:2,5-DibroMo-4-nitropyridine
Synonyms:Pyridine, 2,5-dibromo-4-nitro-
CAS:221241-31-2
MF:C5H2Br2N2O2
MW:281.89
EINECS:
Product Categories:
Mol File:221241-31-2.mol
2,5-DibroMo-4-nitropyridine Structure
2,5-DibroMo-4-nitropyridine Chemical Properties
Boiling point 283.7±35.0 °C(Predicted)
density 2+-.0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-5.49±0.18(Predicted)
AppearanceWhite to light yellow Solid
Safety Information
MSDS Information
2,5-DibroMo-4-nitropyridine Usage And Synthesis
Synthesis
2,5-DIBROMO-4-NITROPYRIDINE 1-OXIDE

221241-25-4

2,5-DibroMo-4-nitropyridine

221241-31-2

General procedure for the synthesis of 2,5-dibromo-4-nitropyridine as 2,5-dibromo-4-nitropyridine nitrogen oxide: 2,5-dibromo-4-nitropyridine nitrogen oxide (18 g, 60.84 mmol) was added batchwise to stirred phosphorus tribromide (46 mL) at 0-5 °C. The reaction mixture was kept stirred at 5 °C for about 7 hours. Upon completion of the reaction, the mixture was slowly poured onto crushed ice and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. Subsequently, the organic phase was concentrated under reduced pressure to give the crude product. Finally, the crude product was purified by fast column chromatography (petroleum ether: ethyl acetate = 10:1) to afford the target compound 2,5-dibromo-4-nitropyridine (10 g, 59% yield).

References[1] Patent: US2014/94456, 2014, A1. Location in patent: Paragraph 0832; 0835
[2] Patent: WO2015/153683, 2015, A1. Location in patent: Paragraph 0624
2,5-DibroMo-4-nitropyridine Preparation Products And Raw materials
Raw materials2,5-DIBROMO-4-NITROPYRIDINE 1-OXIDE
Tag:2,5-DibroMo-4-nitropyridine(221241-31-2) Related Product Information
2,5-DibroMo-4-nitropyridine