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2-(Trifluoromethoxy)bromobenzene

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2-(Trifluoromethoxy)bromobenzene Basic information

Product Name:
2-(Trifluoromethoxy)bromobenzene
Synonyms:
  • 1-Bromo-2-(trifluoromethoxy)benzene 99%
  • 2-Bromo-alpha,alpha,alpha-trifluoroanisole, 2-Bromophenyl trifluoromethyl ether
  • 2-BroMo-1-(trifluoroMethoxy)benzene
  • Dibromoethoxychlorophosphonazo Trifluoromethoxybenzene
  • Adjacent Bromine Trifluoride Mathoxyphenyl
  • 1-BROMO-2-(TRIFLUOROMETHOXY)BENZENE
  • 2-(TRIFLUOROMETHOXY)BENZENE
  • 2-(TRIFLUOROMETHOXY)BROMOBENZENE
CAS:
64115-88-4
MF:
C7H4BrF3O
MW:
241.01
Product Categories:
  • Pyridines
  • alkyl bromide
  • Fluorobenzene
  • Aromatic Halides (substituted)
  • Trifluoroanisole series
  • Miscellaneous
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
Mol File:
64115-88-4.mol
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2-(Trifluoromethoxy)bromobenzene Chemical Properties

Boiling point:
158-160 °C(lit.)
Density 
1.62 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.464(lit.)
Flash point:
140 °F
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow
BRN 
1947768
CAS DataBase Reference
64115-88-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37
RIDADR 
UN1993
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
3
PackingGroup 
III
HS Code 
29093090

MSDS

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2-(Trifluoromethoxy)bromobenzene Usage And Synthesis

General Description

1-Bromo-2-(trifluoromethoxy)benzene can be prepared from (trifluoromethoxy)benzene.

Synthesis

1035797-66-0

88284-48-4

64115-88-4

In a glove box, KF (78.4 mg, 1.35 mmol, 4.5 eq.) was added to a 20 mL polyethylene (PE) plastic tube. Subsequently, dicyclohexane-18-crown-6 (503 mg, 1.35 mmol, 4.5 eq.) and 6. Next, ethylidene precursor (0.3 mmol, 1.0 eq.), 1-bromophenylacetylene (218 mg, 1.2 mmol, 4.0 eq.) or perfluorohexyl bromide (479 mg, 1.2 mmol, 4.0 eq.) or pentafluorophenyl bromide ( 296 mg, 1.2 mmol, 4.0 equiv) and trifluoromethyl benzoate (171 mg, 0.9 mmol, 3.0 equiv). The reaction tube was sealed and the reaction was carried out at room temperature for 12 hours. At the end of the reaction, the F-spectral yield was first determined by 19F NMR. Finally, the reaction mixture was filtered, dried and purified directly by column chromatography.

References

[1] Patent: CN108516935, 2018, A. Location in patent: Paragraph 0166; 0167; 0168; 0169; 0170; 0171
[2] Journal of the American Chemical Society, 2018, vol. 140, # 22, p. 6801 - 6805

2-(Trifluoromethoxy)bromobenzene Preparation Products And Raw materials

Preparation Products

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