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CAS 2096339-99-8

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B-[2-Fluoro-5-hydroxy-3-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-Fluoro-5-hydroxy-3-(trifluoromethyl)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 and other nucleophiles. This compound features a phenyl ring substituted with a fluorine atom, a hydroxyl group, and a trifluoromethyl group, contributing to its unique chemical properties. The trifluoromethyl group enhances lipophilicity and can influence the compound's reactivity and biological activity. The presence of the boronic acid moiety allows for potential applications in medicinal chemistry, particularly in drug design and development, as boronic acids are often used in the synthesis of biologically active compounds and in the development of sensors. Additionally, the fluorine and trifluoromethyl substituents can modulate the electronic properties of the molecule, making it a candidate for various chemical reactions, including Suzuki coupling. Overall, this compound's structure suggests it may have significant utility in both synthetic and pharmaceutical chemistry.
Formula:C7H5BF4O3
InChI:InChI=1S/C7H5BF4O3/c9-6-4(7(10,11)12)1-3(13)2-5(6)8(14)15/h1-2,13-15H
InChI key:InChIKey=WAKPESZATTZWEQ-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(F)C(B(O)O)=CC(O)=C1
Synonyms:
  • B-[2-Fluoro-5-hydroxy-3-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[2-fluoro-5-hydroxy-3-(trifluoromethyl)phenyl]-
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