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1-Bromo-4-(pentafluorosulfanyl)benzene

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1-Bromo-4-(pentafluorosulfanyl)benzene Basic information

Product Name:
1-Bromo-4-(pentafluorosulfanyl)benzene
Synonyms:
  • 4-BROMOPHENYL-PENTAFLUOROSULFUR
  • 4-BROMOPHENYLSULFUR PENTAFLUORIDE
  • 4-BROMOPHENYLSULPHUR PENTAFLUORIDE
  • 1-BROMO-4-(PENTAFLUOROSULFANYL)BENZENE
  • 1-BROMO-4-(PENTAFLUOROTHIO)BENZENE
  • 4-Pentafluorosulfur bromobenzene
  • 1-Bromo-4-(pentafluorothio)benzene, 1-Bromo-4-(pentafluorosulphanyl)benzene
  • 4-BroMophenylsulfur pentafluoride, 95+%
CAS:
774-93-6
MF:
C6H4BrF5S
MW:
283.06
Product Categories:
  • Halides
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
Mol File:
774-93-6.mol
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1-Bromo-4-(pentafluorosulfanyl)benzene Chemical Properties

Boiling point:
77.2 °C(Press: 10 Torr)
refractive index 
1.4790-1.4830
Flash point:
84°C(lit.)
storage temp. 
0-10°C
form 
liquid
color 
Clear, colourless
InChI
InChI=1S/C6H4BrF5S/c7-5-1-3-6(4-2-5)13(8,9,10,11)12/h1-4H
InChIKey
RECCABBXFXGELM-UHFFFAOYSA-N
SMILES
S(F)(F)(F)(F)(F)C1=CC=C(Br)C=C1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
23-26-36/37/39
Hazard Note 
Irritant
HS Code 
2930909899
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1-Bromo-4-(pentafluorosulfanyl)benzene Usage And Synthesis

Synthesis

5.0 g of 4-pentafluorosulfanylaniline was dissolved in 20 ml of acetic acid, and, at 0 ℃, a saturated aqueous HBr solution was added. Then, at 0 ℃, a solution of 1.9 of NaNO2 in 5 ml of water was slowly added dropwise over the course of 5 minutes. The reaction mixture was stirred at 0 C. for 10 minutes and then added in portions to a suspension of 6.5 g of CuBr in 20 ml of a half-saturated aqueous HBr solution at 0 ℃. Nitrogen is liberated during this. The mixture was stirred at 0 ℃. for 30 minutes and then at RT for 1 h. It was subsequently extracted 3 times with 100 ml of HEP each time, and then the HEP was washed twice with 50 ml of a saturated aqueous Na2CO3 solution each time. The residue, after drying over MgSO4 and removal of the solvent in vacuo, was chromatographed on silica gel with HEP. 1.8 g of a colorless oil 1-Bromo-4-(pentafluorosulfanyl)benzene were obtained.

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