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CAS 958457-42-6

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B-[4-[3-(Trifluoromethyl)phenoxy]phenyl]boronic acid

Description:
B-[4-[3-(Trifluoromethyl)phenoxy]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The compound features a trifluoromethyl group, which enhances its lipophilicity and can influence its biological activity. The phenoxy and phenyl groups contribute to its structural complexity and may affect its solubility and reactivity. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the trifluoromethyl group can impart unique electronic properties, potentially affecting the compound's interaction with biological targets. Overall, B-[4-[3-(Trifluoromethyl)phenoxy]phenyl]boronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.
Formula:C13H10BF3O3
InChI:InChI=1S/C13H10BF3O3/c15-13(16,17)9-2-1-3-12(8-9)20-11-6-4-10(5-7-11)14(18)19/h1-8,18-19H
InChI key:InChIKey=CPGMKXOOKRKAFT-UHFFFAOYSA-N
SMILES:O(C1=CC(C(F)(F)F)=CC=C1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, B-[4-[3-(trifluoromethyl)phenoxy]phenyl]-
  • (4-(3-(Trifluoromethyl)phenoxy)phenyl)boronic acid
  • [4-[[3-(Trifluoromethyl)phenyl]oxy]phenyl]boronic acid
  • B-[4-[3-(Trifluoromethyl)phenoxy]phenyl]boronic acid
  • (4-(3-(Trifluoromethyl)phenoxy)phenyl)boronic
  • (4-[3-(Trifluoromethyl)phenoxy]phenyl)boranediol
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