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CAS 1072952-03-4

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B-[3-[(4-Fluorophenyl)methoxy]phenyl]boronic acid

Description:
B-[3-[(4-Fluorophenyl)methoxy]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, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a methoxy group and a fluorophenyl moiety, which can influence its electronic properties and reactivity. The presence of the fluorine atom can enhance the compound's lipophilicity and potentially its biological activity. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the compound may exhibit properties such as solubility in organic solvents and potential interactions with biological targets, making it of interest in drug development and material science. Its specific characteristics, such as melting point, solubility, and reactivity, would typically be determined through experimental studies.
Formula:C13H12BFO3
InChI:InChI=1S/C13H12BFO3/c15-12-6-4-10(5-7-12)9-18-13-3-1-2-11(8-13)14(16)17/h1-8,16-17H,9H2
InChI key:InChIKey=WSTWPQWJAKLITI-UHFFFAOYSA-N
SMILES:O(CC1=CC=C(F)C=C1)C2=CC(B(O)O)=CC=C2
Synonyms:
  • Boronic acid, B-[3-[(4-fluorophenyl)methoxy]phenyl]-
  • B-[3-[(4-Fluorophenyl)methoxy]phenyl]boronic acid
  • [3-[(4-Fluorophenyl)methoxy]phenyl]boronic acid
  • (3-((4-Fluorobenzyl)oxy)phenyl)boronic acid
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