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CAS 2096329-68-7

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B-(2,4-Difluoro-3-propoxyphenyl)boronic acid

Description:
B-(2,4-Difluoro-3-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with two fluorine atoms and a propoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of fluorine atoms can enhance the compound's lipophilicity and influence its biological activity, while the propoxy group may contribute to its solubility and stability in organic solvents. Additionally, boronic acids are known for their role in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Overall, B-(2,4-Difluoro-3-propoxyphenyl)boronic acid is a versatile compound with potential applications in drug development and materials science.
Formula:C9H11BF2O3
InChI:InChI=1S/C9H11BF2O3/c1-2-5-15-9-7(11)4-3-6(8(9)12)10(13)14/h3-4,13-14H,2,5H2,1H3
InChI key:InChIKey=BUFQSDWLWIWVKM-UHFFFAOYSA-N
SMILES:O(CCC)C1=C(F)C(B(O)O)=CC=C1F
Synonyms:
  • B-(2,4-Difluoro-3-propoxyphenyl)boronic acid
  • Boronic acid, B-(2,4-difluoro-3-propoxyphenyl)-
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