Basic information Description Uses Safety Supplier Related

2,3-DIFLUORO-5-(TRIFLUOROMETHYL)PYRIDINE

Basic information Description Uses Safety Supplier Related

2,3-DIFLUORO-5-(TRIFLUOROMETHYL)PYRIDINE Basic information

Product Name:
2,3-DIFLUORO-5-(TRIFLUOROMETHYL)PYRIDINE
Synonyms:
  • 2,3-DIFLUORO-5-(TRIFLUOROMETHYL)PYRIDINE
  • alpha,alpha,alpha,5,6-Pentafluoro-3-picoline
  • 2,3-Difluoro-5-(trifluoromethyl)pyridine >
  • Pyridine, 2,3-difluoro-5-(trifluoromethyl)-
CAS:
89402-42-6
MF:
C6H2F5N
MW:
183.08
Product Categories:
  • alkyl Fluorine
  • OLED
Mol File:
89402-42-6.mol
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2,3-DIFLUORO-5-(TRIFLUOROMETHYL)PYRIDINE Chemical Properties

Melting point:
-20°C
Boiling point:
104°C
Density 
1,47 g/cm3
refractive index 
1.3860-1.3900
Flash point:
28°C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
clear liquid
pka
-5.28±0.20(Predicted)
color 
Colorless to Light yellow to Light orange
InChI
InChI=1S/C6H2F5N/c7-4-1-3(6(9,10)11)2-12-5(4)8/h1-2H
InChIKey
XIFCGIKPAAZFFS-UHFFFAOYSA-N
SMILES
C1(F)=NC=C(C(F)(F)F)C=C1F
CAS DataBase Reference
89402-42-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
10-36-25
Safety Statements 
16-45-26
RIDADR 
1993
Hazard Note 
Harmful
HazardClass 
IRRITANT
HS Code 
2933399990
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2,3-DIFLUORO-5-(TRIFLUOROMETHYL)PYRIDINE Usage And Synthesis

Description

2,3-Difluoro-5-(trifluoromethyl)pyridine is a useful research chemical.

Uses

2,3-Difluoro-5-(trifluoroMethyl)pyridine is a heterocyclic compound and can be used as a pharmaceutical intermediate.

Synthesis

69045-84-7

89402-42-6

The general procedure for the synthesis of 2,3-dichloro-5-trifluoromethylpyridine from 2,3-dichloro-5-trifluoromethylpyridine is as follows: 1500 mL of DMSO, 363 g of cesium fluoride, and 8 g of potassium carbonate were added to a 5000 mL reaction flask and heated in an oil bath. Concentrate and cool 600 mL of DMSO under reduced pressure to below 80 °C. Under nitrogen protection, 318 g (1.58 mol) of 2,3-dichloro-5-trifluoromethylpyridine was added to the reaction system and the reaction was carried out at about 110 °C for 48 hours. After completion of the reaction, 600 mL of water was added to the yellow liquid for liquid-liquid separation. The organic phase was dried with anhydrous magnesium sulfate and filtered to give a crude product of 188 g. The 100-102 °C fractions were collected by distillation to give 139 g of 2,3-difluoro-5-trifluoromethylpyridine in 47.6% yield.

References

[1] Patent: CN104628679, 2018, B. Location in patent: Paragraph 0061; 0064; 0065
[2] Patent: US2008/221327, 2008, A1. Location in patent: Page/Page column 6; 9

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