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2-(Trifluoromethoxy)bromobenzene

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CAS:64115-88-4
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CAS:64115-88-4
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2-(Trifluoromethoxy)bromobenzene manufacturers

2-(Trifluoromethoxy)bromobenzene Basic information
Product Name:2-(Trifluoromethoxy)bromobenzene
Synonyms:2-Bromo-6-(trifluoromethyl)anisole;1-BroMo-2-(trifluoroMethoxy)benzen1-BroMo-2-(trifluoroMethoxy)benzen;2-Bromo-alpha,alpha,alpha-trifluoroanisole, 1-Bromo-2-(trifluoromethoxy)benzene, 2-Bromophenyl trifluoromethyl ether;light yellow liquid,bp185;1-Bromo-2-(trifluoromethoxy)benzene 99%;2-Bromo-alpha,alpha,alpha-trifluoroanisole, 2-Bromophenyl trifluoromethyl ether;2-BroMo-1-(trifluoroMethoxy)benzene;Dibromoethoxychlorophosphonazo Trifluoromethoxybenzene
CAS:64115-88-4
MF:C7H4BrF3O
MW:241.01
EINECS:
Product Categories:Pyridines;alkyl bromide;Trifluoroanisole series;Fluorobenzene;Aromatic Halides (substituted);Miscellaneous;Ethers;Organic Building Blocks;Oxygen Compounds
Mol File:64115-88-4.mol
2-(Trifluoromethoxy)bromobenzene Structure
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.)
Fp 140 °F
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow
BRN 1947768
InChI1S/C7H4BrF3O/c8-5-3-1-2-4-6(5)12-7(9,10)11/h1-4H
InChIKeyITYCJCVRPBLODP-UHFFFAOYSA-N
SMILESFC(F)(F)Oc1ccccc1Br
CAS DataBase Reference64115-88-4(CAS DataBase Reference)
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
Storage Class3 - Flammable liquids
Hazard ClassificationsFlam. Liq. 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2-(Trifluoromethoxy)bromobenzene Usage And Synthesis
Uses1-Bromo-2-(trifluoromethoxy)benzene can be prepared from (trifluoromethoxy)benzene.
General Description1-Bromo-2-(trifluoromethoxy)benzene can be prepared from (trifluoromethoxy)benzene.
Synthesis
trifluoromethyl benzoate

1035797-66-0

2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE

88284-48-4

2-(Trifluoromethoxy)bromobenzene

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
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