Identification | Back Directory | [Name]
2-(TRIFLUOROMETHYL)PHENACYL BROMIDE | [CAS]
54109-16-9 | [Synonyms]
2-(TRIFLUOROMETHYL)PHENACYL BROMIDE 2-(trifluoromethtl)phenacyl bromide 2'-(TRIFLUOROMETHYL)PHENACYL BROMIDE 2-Bromo-2'-(trifluoromethyl)acetophenone 2-Bromo-2'-(trifluoromethyl)acetophenone > 2-Bromo-2'-(trifluoromethyl)acetophenone,97% 2-Bromo-1-(2-trifluoromethyl-phenyl)-ethanone Ethanone, 2-bromo-1-[2-(trifluoromethyl)phenyl]- 2-BROMO-1-[2-(TRIFLUOROMETHYL)PHENYL]-1-ETHANONE 2-Bromo-1-[2-(trifluoromethyl)phenyl]-1-ethanone, 95+% 2-Bromo-2'-(trifluoromethyl)acetophenone, 2-Bromo-1-[2-(trifluoromethyl)phenyl]ethan-1-one | [Molecular Formula]
C9H6BrF3O | [MDL Number]
MFCD03094304 | [MOL File]
54109-16-9.mol | [Molecular Weight]
267.04 |
Chemical Properties | Back Directory | [Melting point ]
28-30 | [Boiling point ]
52/0.03mm | [density ]
1.592±0.06 g/cm3 (20 ºC 760 Torr) | [Fp ]
109.7±27.3℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [Water Solubility ]
Slightly soluble in water. | [CAS DataBase Reference]
54109-16-9 |
Hazard Information | Back Directory | [Uses]
The sulfonyl urea thus obtained was used directly in the following condensation with 4-(trifluoromethyl)phenacyl bromide. Upon heating, benzenesulfinic acid ammonium salt might react with 2-(trifluoromethyl)phenacyl bromide to give β-keto sulfone. In Rap-Stoermer condensation reation. |
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