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CAS 958451-74-6

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B-[3-(Difluoromethoxy)-4-methylphenyl]boronic acid

Description:
B-[3-(Difluoromethoxy)-4-methylphenyl]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, including organic synthesis and medicinal chemistry. The compound features a difluoromethoxy group, which enhances its electronic properties and may influence its reactivity and solubility. The methyl group on the phenyl ring contributes to its steric and electronic characteristics, potentially affecting its interactions in chemical reactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its boronic acid functionality allows it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of fluorine atoms can impart unique properties, such as increased lipophilicity and altered biological activity, which are of interest in pharmaceutical development. Overall, B-[3-(Difluoromethoxy)-4-methylphenyl]boronic acid is a versatile compound with significant implications in synthetic and medicinal chemistry.
Formula:C8H9BF2O3
InChI:InChI=1S/C8H9BF2O3/c1-5-2-3-6(9(12)13)4-7(5)14-8(10)11/h2-4,8,12-13H,1H3
InChI key:InChIKey=WVVOHJNTNLIDIK-UHFFFAOYSA-N
SMILES:O(C(F)F)C1=CC(B(O)O)=CC=C1C
Synonyms:
  • B-[3-(Difluoromethoxy)-4-methylphenyl]boronic acid
  • Boronic acid, B-[3-(difluoromethoxy)-4-methylphenyl]-
  • 3-difluoromethoxy-4-methyl-benzeneboronic acid
  • [3-(difluoromethoxy)-4-methylphenyl]boronic acid
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