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3-Bromo-4-nitropyridine

3-Bromo-4-nitropyridine Suppliers list
Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:3-bromo-4-nitropyridine
CAS:89364-04-5
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: CAS:89364-04-5
Purity:98% Package:g-Kg
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Products Intro: Product Name:3-BROMO-4-NITROPYRIDINE
CAS:89364-04-5
Purity:98% Package:1kg;1USD
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Products Intro: Product Name:3-Bromo-4-nitropyridine
CAS:89364-04-5
Purity:>=97% Package:1g;5g;10g;25g;100g;500g
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Products Intro: Product Name:3-BROMO-4-NITROPYRIDINE
CAS:89364-04-5

3-Bromo-4-nitropyridine manufacturers

3-Bromo-4-nitropyridine Basic information
Uses
Product Name:3-Bromo-4-nitropyridine
Synonyms:IFLAB-BB F1371-0211;3-BROMO-4-NITROPYRIDINE;i3-Bromo-4-nitropyridine;Pyridine, 3-bromo-4-nitro-;3-BROMO-4-NITROPYRIDINE 97%;3-BROMO-4-NITROPYRIDINE ISO 9001:2015 REACH;Flortaucipir Impurity 26
CAS:89364-04-5
MF:C5H3BrN2O2
MW:202.99
EINECS:
Product Categories:Pyridines
Mol File:89364-04-5.mol
3-Bromo-4-nitropyridine Structure
3-Bromo-4-nitropyridine Chemical Properties
Melting point 66-67 °C
Boiling point 235.7±20.0 °C(Predicted)
density 1.833±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-1.04±0.18(Predicted)
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C5H3BrN2O2/c6-4-3-7-2-1-5(4)8(9)10/h1-3H
InChIKeyCJEWCWSWUUFORD-UHFFFAOYSA-N
SMILESC1=NC=CC([N+]([O-])=O)=C1Br
Safety Information
HS Code 2933399990
MSDS Information
3-Bromo-4-nitropyridine Usage And Synthesis
Uses3-Bromo-4-nitropyridine is a pyridine compound that has been identified as an environmental pollutant. It can be used to synthesize other compounds, such as 4-(3-bromopyridin-2-yl)morpholine, for the synthesis of acetonitrile.
SynthesisA mixture of 3-bromo-4-nitropyridine N-oxide (2.2g,10 mmol), trichlorooxobis (triphenylphosphine) rhenium(V) [Re(0)(Ph3P)2Cl3, Aldrich, 50 mg, 0.08mmol), and triphenyphosphine (2.7 g, 10.3 mmol) in dichloromethane (100 mL) was flushed with argon and stirred at rt for 1 h, then, at 40 °C for 2 h. The reaction mixture was cooled to rt and concentrated under vacuum. The residue was triturated with hexanes (300 mL), and the precipitated (triphenylphosphine oxide) was removed by filtration. The organic layer was concentrated and purified by column (silica gel, EtOAc/hexanes 1/7) to give 3-Bromo-4-nitropyridine as yellow solid (1.8 g, 86%)[1].
References[1] R. W. Daisley, J. R. Hanbali. “PREPARATION OF 3-BROMO-4-NITROPYRIDINE 1-OXIDE.” Organic Preparations and Procedures International 15 1 (1983): 280–282.
3-Bromo-4-nitropyridine Preparation Products And Raw materials
Preparation Products1533432-50-6-->3-Fluoro-4-nitropyridine-->3-BROMO-4-FLUOROPYRIDINE-->3-BroMo-4-chloro-pyridine 1-oxide
Tag:3-Bromo-4-nitropyridine(89364-04-5) Related Product Information
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