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CAS 849052-16-0

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

Description:
B-[3-Bromo-2-[(3-bromophenyl)methoxy]-5-methylphenyl]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. This compound features a complex aromatic structure, including bromine substituents and a methoxy group, which contribute to its chemical reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of bromine atoms enhances its electrophilic character, making it useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the boronic acid moiety allows for the formation of boronate esters, facilitating further transformations. This compound may exhibit biological activity, making it of interest in drug discovery and development. Its solubility and stability in various solvents can vary, influencing its practical applications in laboratory settings. Overall, this compound represents a versatile building block in synthetic organic chemistry.
Formula:C14H13BBr2O3
InChI:InChI=1S/C14H13BBr2O3/c1-9-5-12(15(18)19)14(13(17)6-9)20-8-10-3-2-4-11(16)7-10/h2-7,18-19H,8H2,1H3
InChI key:InChIKey=VWXCNKUTFMOYDY-UHFFFAOYSA-N
SMILES:O(CC1=CC(Br)=CC=C1)C2=C(B(O)O)C=C(C)C=C2Br
Synonyms:
  • Boronic acid, B-[3-bromo-2-[(3-bromophenyl)methoxy]-5-methylphenyl]-
  • Boronic acid, [3-bromo-2-[(3-bromophenyl)methoxy]-5-methylphenyl]-
  • B-[3-Bromo-2-[(3-bromophenyl)methoxy]-5-methylphenyl]boronic acid
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