2-Bromo-5-chlorobenzotrifluoride
2-Bromo-5-chlorobenzotrifluoride Basic information
- Product Name:
- 2-Bromo-5-chlorobenzotrifluoride
- Synonyms:
-
- Benzene,2-bromo-5-chloro-1-(trifluoromethyl)-
- 2-bromo-5-chloro-α,α,α-trifluorotoluene
- 2-Bromo-5-chlorobenzotrifluoride 99%
- 2-Bromo-5-chlorobenzotrifluoride99%
- 2-BROMO-5-CHLOROBENZOTRIFLUORIDE, 98+%
- 1-Bromo-4-chloro-2-(trifluoromethyl)benzene
- 2-Bromo-5-chlorobenzotrifluoride,2-Bromo-5-chloro-α,α,α-trifluorotoluene
- 2-BroMo-5-chlorozotrifluoride
- CAS:
- 344-65-0
- MF:
- C7H3BrClF3
- MW:
- 259.45
- EINECS:
- 608-994-3
- Product Categories:
-
- Bromine Compounds
- Chlorine Compounds
- Fluorine Compounds
- Mol File:
- 344-65-0.mol
2-Bromo-5-chlorobenzotrifluoride Chemical Properties
- Melting point:
- 18-20°C
- Boiling point:
- 179-180 °C (lit.)
- Density
- 1.759 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.5080(lit.)
- Flash point:
- 198°C
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- clear liquid
- color
- Colorless to Almost colorless
- BRN
- 2448030
- CAS DataBase Reference
- 344-65-0(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39-36-37-23
- WGK Germany
- 3
- Hazard Note
- Irritant
- HS Code
- 29039990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
2-Bromo-5-chlorobenzotrifluoride Usage And Synthesis
Chemical Properties
Clear colourless to slightly yellow liquid
Uses
2-Bromo-5-chlorobenzotrifluoride was used in preparation of 6-[4-chloro-2-(trifluoromethyl)phenyl]-3-fluoro-2-methylpyridine and 4,4′-dichloro-2,2′-bis(trifluoromethyl) diphenyl sulphone.
Synthesis
393-36-2
344-65-0
The general procedure for synthesizing 2-bromo-5-chlorobenzotrifluoride from 5-amino-2-bromobenzotrifluoride was as follows: a diazonium salt solution was prepared according to the method described in Example 3. The cooled diazonium salt solution was slowly added to a pre-stirred and cooled mixture of CuCl (8.9 g, 0.091 mol) dissolved in concentrated hydrochloric acid (46 g, 0.44 mol). The reaction system was kept at a low temperature and when the addition was completed, it was gradually warmed up to room temperature with continuous stirring for 2 to 3 hours. Subsequently, the reaction mixture was heated to 60-70 °C to ensure complete reaction. Upon completion of the reaction, the target product 2-bromo-5-chlorobenzotrifluoride was obtained by isolation by appropriate methods. Yield: 65%.
References
[1] Patent: WO2016/63300, 2016, A1. Location in patent: Page/Page column 8
[2] Journal of the American Chemical Society, 1953, vol. 75, p. 3034
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2-Bromo-5-chlorobenzotrifluoride(344-65-0)Related Product Information
- 3-Chlorobenzotrifluoride
- 2-Fluoro-5-bromobenzotrifluoride
- Benzotrifluoride
- 3-BROMO-4-CHLOROBENZOTRIFLUORIDE
- 4-AMINO-3-BROMO-5-CHLOROBENZOTRIFLUORIDE
- 3-BROMO-2-CHLOROBENZOTRIFLUORIDE
- 2-Bromo-5-chlorobenzotrifluoride
- 4-Bromochlorobenzene
- 1-Bromo-4-chloro-2-methylbenzene
- 3-BROMO-6-CHLOROBENZOTRIFLUORIDE,5-BROMO-2-CHLOROBENZOTRIFLUORIDE
- 2-BROMO-6-CHLOROBENZOTRIFLUORIDE
- 4-BROMO-3-CHLOROBENZOTRIFLUORIDE
- 2-AMINO-3-BROMO-5-CHLOROBENZOTRIFLUORIDE
- 1-Bromo-2-difluoromethylbenzene
- 2,3-Dibromo-5-chlorobenzotrifluoride
- 2-BROMO-3-CHLOROBENZOTRIFLUORIDE
- 2-AMINO-5-BROMO-3-CHLOROBENZOTRIFLUORIDE
- 4-BROMO-2-CHLOROBENZOTRIFLUORIDE