2-(Trifluoromethoxy)bromobenzene
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
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)
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
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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
2-(Trifluoromethoxy)bromobenzeneSupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
- Tel
- 400-6106006
- saleschina@alfa-asia.com
- Tel
- +86 351 7031519
- sales@RHFChem.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
2-(Trifluoromethoxy)bromobenzene(64115-88-4)Related Product Information
- 4-(Trifluoromethoxy)chlorobenzene
- 2-Methylbenzotrifluoride
- 3-(Trifluoromethoxy)aniline
- 4-(Trifluoromethoxy)benzaldehyde
- 2-Fluorobenzoyl chloride
- 4'-(Trifluoromethoxy)acetophenone
- 4-Bromofluorobenzene
- 2-Bromofluorobenzene
- Guaiacol
- 2-(Trifluoromethyl)benzaldehyde
- Methyl 2-bromobenzoate
- Bromobenzene
- Bromoxynil
- 3-(METHOXYMETHOXY)BENZALDEHYDE
- (Trifluoromethoxy)benzene
- 3-Bromofluorobenzene
- p-Anisaldehyde
- 2-(Trifluoromethoxy)aniline