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4-Fluoropyridine hydrochloride

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4-Fluoropyridine hydrochloride Basic information

Product Name:
4-Fluoropyridine hydrochloride
Synonyms:
  • 4-FLUOROPYRIDINE HCL
  • 4-FLUOROPYRIDINE HYDROCHLORIDE
  • 4-Fluoropyridine HCl Salt
  • 4-FLUOROPYRIDINE HYDROCHLORIDE, 99.0% MIN.
  • 4-fluoropyridine hydrochlorate
  • 4-Fluoropyridine hydrochloride ,98%
  • 4-Fluoropyridine hyd
  • 4-Fluoropyridine hydrochloride 98%
CAS:
39160-31-1
MF:
C5H5ClFN
MW:
133.55
EINECS:
630-984-2
Product Categories:
  • Fluoropyridines
  • Halopyridines
  • Fluorinated heterocyclic series
  • Pyridines
  • API intermediates
  • Pyridine
  • Halides
Mol File:
39160-31-1.mol
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4-Fluoropyridine hydrochloride Chemical Properties

Melting point:
100 °C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Water Solubility 
Soluble in water
form 
powder to crystal
color 
White to Almost white
InChI
1S/C5H4FN.ClH/c6-5-1-3-7-4-2-5;/h1-4H;1H
InChIKey
QRUIPALQRYLTAF-UHFFFAOYSA-N
SMILES
Cl.Fc1ccncc1
CAS DataBase Reference
39160-31-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29333990
Storage Class
11 - Combustible Solids
Hazard Classifications
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
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4-Fluoropyridine hydrochloride Usage And Synthesis

Chemical Properties

Light yellow powder.

Uses

4-Fluoropyridine Hydrochloride is the salt version of 4-Fluoropyridine (B439463(M)), which was useful for studying the interaction of pyridines with OCS.

Synthesis

A suspension of 4-aminopyridine (7.06 g, 75.1 mmol) in 40 mL of anhydrous dichloromethane was stirred at -78??C for 15 min. minutes and added to anhydrous HF (31.2 g, 1.6 ) that had been cooled to -78??C in a polyethylene vial. mol). The reaction mixture was allowed to warm to -5??C and NaNO2 was added in batches over 10 min. (6.22 g, 90.1 mmol) while maintaining the temperature between -5 and 0??C. The mixture was allowed to warm to room temperature and then heated to 40-50??C for 1.5 hours. Dichloromethane (50 mL) was added. After cooling to -10??C, adjust pH to 10 by dropwise addition of 30% aqueous NH4OH over 10 min. filter to break emulsion and extract with dichloromethane. After drying on silica gel, HCl gas was bubbled through the solution. The solvent was evaporated in vacuum to give 4.9 g (37.1 mmol, 50%) of a pale yellow salt.

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