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CAS 1072946-32-7

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B-[2,4-Dichloro-3-(phenylmethoxy)phenyl]boronic acid

Description:
B-[2,4-Dichloro-3-(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 chemical applications, including organic synthesis and medicinal chemistry. The compound features a dichlorophenyl moiety, which contributes to its reactivity and potential biological activity. The phenylmethoxy group enhances its solubility and stability in organic solvents. This compound is typically utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, boronic acids are often explored for their role in drug development, particularly in targeting specific biological pathways. The presence of chlorine substituents can influence the electronic properties and reactivity of the molecule, making it a subject of interest in the design of new materials and pharmaceuticals. Overall, B-[2,4-Dichloro-3-(phenylmethoxy)phenyl]boronic acid exemplifies the versatility of boron-containing compounds in modern chemistry.
Formula:C13H11BCl2O3
InChI:InChI=1S/C13H11BCl2O3/c15-11-7-6-10(14(17)18)12(16)13(11)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
InChI key:InChIKey=ISXBLZCSJKQVQQ-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(Cl)C(B(O)O)=CC=C2Cl
Synonyms:
  • Boronic acid, B-[2,4-dichloro-3-(phenylmethoxy)phenyl]-
  • B-[2,4-Dichloro-3-(phenylmethoxy)phenyl]boronic acid
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