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CAS 1092461-36-3

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3-Bromo-5-(trifluoromethoxy)benzoyl chloride

Description:
3-Bromo-5-(trifluoromethoxy)benzoyl chloride is an organic compound characterized by its functional groups and structural features. It contains a benzoyl chloride moiety, which is a derivative of benzoic acid where the hydroxyl group is replaced by a chlorine atom. The presence of a bromine atom at the 3-position and a trifluoromethoxy group at the 5-position on the benzene ring contributes to its unique reactivity and properties. The trifluoromethoxy group is known for its electron-withdrawing characteristics, which can enhance the electrophilicity of the carbonyl carbon in the benzoyl chloride. This compound is typically used in organic synthesis, particularly in the preparation of more complex molecules, due to its ability to participate in various chemical reactions, such as acylation and nucleophilic substitutions. Additionally, its fluorinated substituents may impart specific physical properties, such as increased lipophilicity or altered solubility in organic solvents. Safety precautions should be observed when handling this compound, as it may be hazardous due to the presence of reactive functional groups.
Formula:C8H3BrClF3O2
InChI:InChI=1S/C8H3BrClF3O2/c9-5-1-4(7(10)14)2-6(3-5)15-8(11,12)13/h1-3H
InChI key:InChIKey=PRRWHYQCMQADHB-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(C(Cl)=O)=CC(Br)=C1
Synonyms:
  • 3-Bromo-5-(trifluoromethoxy)benzoyl chloride
  • Benzoyl chloride, 3-bromo-5-(trifluoromethoxy)-
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