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3-Bromo-5-fluoropyridine

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CAS:407-20-5
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CAS:407-20-5
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3-Bromo-5-fluoropyridine manufacturers

  • 3-Bromo-5-fluoropyridine
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  • $5.00 / 1KG
  • 2025-09-25
  • CAS:407-20-5
  • Min. Order: 1KG
  • Purity: 98%
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3-Bromo-5-fluoropyridine Basic information
Product Name:3-Bromo-5-fluoropyridine
Synonyms:3-broMine-5-fluoride Pyridine;5 - pyridine broMide - 3 - fluorine;5-broMo-3-fluoride pyridine;Pyridine, 3-bromo-5-fluoro-;5-BROMO-3-FLUOROPYRIDINE;3-BROMO-5-FLUOROPYRIDINE;3-bromo-5-fluoropyridin;3-Bromo-5-fluoropyridine98%
CAS:407-20-5
MF:C5H3BrFN
MW:175.99
EINECS:
Product Categories:C5Heterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;CHIRAL CHEMICALS;Boronic Acid;Fluorinated;Organohalides;Bromopyridines;Fluoropyridines;Halopyridines;Halides;Pyridines derivates;Heterocyclic Compounds;Fluorine series;Pyridine Series;blocks;Bromides;Pyridines;Pyridine;Fluorin-contained pyridine series;bc0001
Mol File:407-20-5.mol
3-Bromo-5-fluoropyridine Structure
3-Bromo-5-fluoropyridine Chemical Properties
Melting point 24-28 °C
Boiling point 78 °C / 11mmHg
density 1.707±0.06 g/cm3(Predicted)
Fp 148 °F
storage temp. Inert atmosphere,Room Temperature
pka0.45±0.20(Predicted)
form Low Melting Solid or Liquid
color Colorless to white
InChIInChI=1S/C5H3BrFN/c6-4-1-5(7)3-8-2-4/h1-3H
InChIKeyHNNNBQRRIHKFLI-UHFFFAOYSA-N
SMILESC1=NC=C(F)C=C1Br
CAS DataBase Reference407-20-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi,F
Risk Statements 22-37/38-41-36/37/38-20/21/22-10
Safety Statements 26-39-36-16
RIDADR UN2811
WGK Germany 3
Hazard Note Irritant
HazardClass 6.1
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
3-Bromo-5-fluoropyridine Usage And Synthesis
Chemical PropertiesColorless liquid
Synthesis
3-Amino-5-bromopyridine

13535-01-8

3-Bromo-5-fluoropyridine

407-20-5

Step 2: Synthesis of 3-bromo-5-fluoropyridine To a cooled solution of 10.0 g (0.058 mol) of 3-amino-5-bromopyridine dissolved in 59 mL of 50% tetrafluoroboric acid was added dropwise at -10 °C a solution prepared from 4.19 g (0.06 mol) of sodium nitrite dissolved in 13 mL of water. The reaction mixture was stirred at -8°C for 1 hr and then 150 mL of ether was added. The crude diazonium salt was collected by filtration and washed with ether. Subsequently, the crude diazonium salt was added in batches to 200 mL of toluene preheated to 80°C. The reaction mixture was stirred at 90°C for 1 hour and then the organic phase was concentrated. The light yellow residue was suspended in 150 mL of water and the pH was adjusted with 32% sodium hydroxide solution to 11. The aqueous phase was extracted three times with 200 mL of dichloromethane. The organic phases were combined, washed with water, dried over magnesium sulfate, and concentrated. The crude product was purified by vacuum distillation (10 mbar, 35 °C) to give 15.4 g of brown oil, which was further purified to give 5.6 g (0.032 mol, 55% yield) of the target compound 3-bromo-5-fluoropyridine as a colorless oil (ISP): m/e = 176.1, 178.1 (M + H+).

References[1] Patent: US2006/199960, 2006, A1. Location in patent: Page/Page column 21
[2] Recueil des Travaux Chimiques des Pays-Bas, 1955, vol. 74, p. 1062,1068
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