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ChemicalBook--->CAS DataBase List--->169222-42-8

169222-42-8

169222-42-8 Structure

169222-42-8 Structure
IdentificationBack Directory
[Name]

4-(Trifluoromethoxy)phenylmagnesium bromide
[CAS]

169222-42-8
[Synonyms]

4-(Trifluoromethoxy)phenylmagnesium bromide
Magnesium, bromo[4-(trifluoromethoxy)phenyl]-
4-(Trifluoromethoxy)phenylmagnesium bromide solution
4-(Trifluoromethoxy)phenylmagnesium bromide 0.5M in 2-MeTHF
(4-(Trifluoromethoxy)phenyl)magnesium bromide, 0.50 M in THF
(4-(Trifluoromethoxy)phenyl)magnesium bromide, 0.50 M in 2-MeTHF
4-(Trifluoromethoxy)phenylmagnesium bromide solution 0.5 M in THF
[Molecular Formula]

C7H4BrF3MgO
[MDL Number]

MFCD09842767
[MOL File]

169222-42-8.mol
[Molecular Weight]

265.31
Chemical PropertiesBack Directory
[density ]

0.975 g/mL at 25 °C
[Fp ]

-30 °C
Safety DataBack Directory
[Symbol(GHS) ]


GHS02, GHS05, GHS07, GHS08
[Signal word ]

Danger
[Hazard statements ]

H225-H302-H314-H335-H351
[Precautionary statements ]

P210-P260-P280-P305+P351+P338-P370+P378-P403+P235
[Hazard Codes ]

F,C
[Risk Statements ]

11-14-19-34-40-37
[Safety Statements ]

16-26-36/37/39-45
[RIDADR ]

UN 2924 3/PG 2
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Reactant for:
  • Preparation of chromanol derivatives as novel class of CETP inhibitors for treatment of cardiovascular disease
  • Pd-catalyzed cross coupling
  • Preparation of indazole-pyridine derivatives as protein kinase B/Akt inhibitors with reduced hypotension, via Stille coupling, Mitsunobu reaction and copper-catalyzed aziridine ring-opening reaction
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