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CAS 849062-40-4

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B-[3-Bromo-2-[(3-fluorophenyl)methoxy]-5-methylphenyl]boronic acid

Description:
B-[3-Bromo-2-[(3-fluorophenyl)methoxy]-5-methylphenyl]boronic acid, identified by its CAS number 849062-40-4, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that features both a bromine and a fluorine substituent. This compound typically exhibits properties associated with 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 the bromine and fluorine substituents can influence its reactivity and solubility, while the methoxy group enhances its electronic properties. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The compound's structural features suggest potential applications in drug development and materials science, particularly in the synthesis of complex organic molecules. As with many boronic acids, it may also exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions.
Formula:C14H13BBrFO3
InChI:InChI=1S/C14H13BBrFO3/c1-9-5-12(15(18)19)14(13(16)6-9)20-8-10-3-2-4-11(17)7-10/h2-7,18-19H,8H2,1H3
InChI key:InChIKey=NOUJKVHYFUPYNQ-UHFFFAOYSA-N
SMILES:O(CC1=CC(F)=CC=C1)C2=C(B(O)O)C=C(C)C=C2Br
Synonyms:
  • B-[3-Bromo-2-[(3-fluorophenyl)methoxy]-5-methylphenyl]boronic acid
  • Boronic acid, B-[3-bromo-2-[(3-fluorophenyl)methoxy]-5-methylphenyl]-
  • Boronic acid, [3-bromo-2-[(3-fluorophenyl)methoxy]-5-methylphenyl]-
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