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CAS 2096340-08-6

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B-[3-Chloro-5-fluoro-4-(phenylmethoxy)phenyl]boronic acid

Description:
B-[3-Chloro-5-fluoro-4-(phenylmethoxy)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 phenylmethoxy group, which enhances its lipophilicity and may influence its biological activity. The presence of chlorine and fluorine substituents on the aromatic ring can significantly affect the compound's electronic properties and reactivity, potentially enhancing its pharmacological profile. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the specific structural features of this compound may contribute to its selectivity and efficacy in targeting certain biological pathways or receptors. Overall, B-[3-Chloro-5-fluoro-4-(phenylmethoxy)phenyl]boronic acid represents a versatile building block in the development of pharmaceuticals and agrochemicals.
Formula:C13H11BClFO3
InChI:InChI=1S/C13H11BClFO3/c15-11-6-10(14(17)18)7-12(16)13(11)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
InChI key:InChIKey=XZMSEOVVBRATJN-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(Cl)C=C(B(O)O)C=C2F
Synonyms:
  • B-[3-Chloro-5-fluoro-4-(phenylmethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-5-fluoro-4-(phenylmethoxy)phenyl]-
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