2-(Trifluoromethoxy)benzoyl chloride, with the CAS number 116827-40-8, is an organic compound characterized by the presence of a benzoyl chloride functional group and a trifluoromethoxy substituent. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. It is known for its reactivity, particularly due to the presence of the acyl chloride functional group, which can readily participate in nucleophilic acyl substitution reactions. The trifluoromethoxy group enhances the compound's electrophilicity and can influence its solubility and stability in various solvents. Additionally, this compound is often utilized in organic synthesis, particularly in the preparation of fluorinated compounds and pharmaceuticals. Due to the presence of chlorine and fluorine atoms, it may exhibit specific environmental and safety considerations, necessitating careful handling and storage. Overall, 2-(Trifluoromethoxy)benzoyl chloride is a valuable intermediate in synthetic organic chemistry.

2-(Trifluoromethoxy)benzoyl chloride

116827-40-8: 2-(Trifluoromethoxy)benzyl chloride, O-Trifluoromethoxybenzoyl chloride, 2-(Trifluoromethoxy)Benzene-1-Carbonyl Chloride, (2,6-Difluorophenyl)Boronic Acid

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CAS 116827-40-8: 2-(Trifluoromethoxy)benzoyl chloride

1-(Chloromethyl)-2-(trifluoromethoxy)benzene

Ref: 3D-FC117096

Benzene, 1-(chloromethyl)-2-(trifluoromethoxy)-

Ref: IN-DA000DAG

2-(Trifluoromethoxy)benzyl chloride

Ref: 54-PC7438UE

1-(Chloromethyl)-2-(trifluoromethoxy)benzene

Ref: 10-F319446