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1-Chloro-2,5-difluorobenzene

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1-Chloro-2,5-difluorobenzene Basic information

Product Name:
1-Chloro-2,5-difluorobenzene
Synonyms:
  • Benzene,2-chloro-1,4-difluoro-
  • 2-CHLORO-1,4-DIFLUOROBENZENE
  • 2,5-DIFLUOROCHLOROBENZENE
  • 1-CHLORO-2,5-DIFLUOROBENZENE
  • 1-CHLORO-2 5-DIFLUOROBENZENE 98%
  • 1-Chloro-2,5-difluorobenzene, 98% [2-Chloro-1,4-difluorobenzene]
  • 1-Chloro-2,5-difluorobenzene98%
  • 1-Chloro-2,5-difluor
CAS:
2367-91-1
MF:
C6H3ClF2
MW:
148.54
EINECS:
624-315-3
Product Categories:
  • Aryl
  • Halogenated Hydrocarbons
  • C6
Mol File:
2367-91-1.mol
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1-Chloro-2,5-difluorobenzene Chemical Properties

Melting point:
24.6 °C
Boiling point:
126-128 °C(lit.)
Density 
1.352 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.478(lit.)
Flash point:
68 °F
storage temp. 
2-8°C
form 
liquid
color 
Clear, faint yellow
BRN 
2081082
CAS DataBase Reference
2367-91-1(CAS DataBase Reference)
NIST Chemistry Reference
1-Chloro-2,5-difluorobenzene(2367-91-1)
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Safety Information

Hazard Codes 
Xn,F,Xi
Risk Statements 
10-20/21/22-36/37-36/37/38-11
Safety Statements 
16-26-36-37/39
RIDADR 
UN 1993 3/PG 2
WGK Germany 
3
Hazard Note 
Flammable
HazardClass 
3
PackingGroup 
III
HS Code 
2903998090

MSDS

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1-Chloro-2,5-difluorobenzene Usage And Synthesis

Chemical Properties

Colorless liquid

Synthesis

108-90-7

348-51-6

352-33-0

625-98-9

1435-44-5

696-02-6

2367-91-1

GENERAL STEPS: In a FEP or PFA reactor fitted with a PTFE-lined magnetic stirring bar and connected to a gas scrubber bottle, substituted benzene (0.95-1.10 mmol), 1,1,1,3,3-pentafluorobutane (2 ml per ml of C6H5R), and BF3-Et2O (1.3-1.5 mmol per mmol C6H5R) were added. The mixture was stirred at 0-5 °C (ice bath) for 10-15 min, followed by batchwise addition of XeF2 (1.2-1.3 mmol per mmol C6H5R). After each addition, the mixture was stirred at 22-25 °C for 3-5 min and cooled to 0-5 °C again. After the addition was completed, the dark colored solution was continued to be stirred at 22-25°C for 15-30 minutes. At the end of the reaction, the reaction was quenched by the addition of 10% aqueous KHCO3, the upper organic layer was separated and filtered through a short column packed with silica gel (40-60 μm). The organic layer was dried with magnesium sulfate and analyzed by 19F NMR and GC/MS. The major products are listed in the table and the others are as follows (GC/MS data).

References

[1] Russian Journal of Organic Chemistry, 2016, vol. 52, # 10, p. 1400 - 1407
[2] Zh. Org. Khim., 2016, vol. 52, # 10, p. 1412 - 1419,8

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