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CAS 480438-59-3

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B-[4-Fluoro-2-(1-methylethoxy)phenyl]boronic acid

Description:
B-[4-Fluoro-2-(1-methylethoxy)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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a fluorinated phenyl ring, which can influence its electronic properties and reactivity. The presence of the 1-methylethoxy group enhances its solubility and stability in organic solvents. This compound is typically used in organic synthesis and medicinal chemistry, where boronic acids play a crucial role in the development of pharmaceuticals and agrochemicals. Its unique structure allows for potential applications in materials science and catalysis. Additionally, the fluorine atom can impart specific characteristics such as increased lipophilicity or altered biological activity, making it a valuable compound for research and development in various fields. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.
Formula:C9H12BFO3
InChI:InChI=1S/C9H12BFO3/c1-6(2)14-9-5-7(11)3-4-8(9)10(12)13/h3-6,12-13H,1-2H3
InChI key:InChIKey=RSEFJQODCQCGRB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC(C)C)C=C(F)C=C1
Synonyms:
  • [4-Fluoro-2-[(propan-2-yl)oxy]phenyl]boronic acid
  • Boronic acid, B-[4-fluoro-2-(1-methylethoxy)phenyl]-
  • 4-Fluoro-2-isopropoxyphenylboronic acid
  • B-[4-Fluoro-2-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, [4-fluoro-2-(1-methylethoxy)phenyl]-
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