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CAS 1256346-47-0

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B-[2,4-Dichloro-5-(phenylmethoxy)phenyl]boronic acid

Description:
B-[2,4-Dichloro-5-(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 dichloro substituents on the aromatic ring contribute to its electronic properties and reactivity. Typically, boronic acids are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of chlorine atoms can affect the compound's solubility and stability in different solvents. Overall, B-[2,4-Dichloro-5-(phenylmethoxy)phenyl]boronic acid is a versatile compound with potential applications in drug development and materials science, owing to its unique structural features and reactivity profile.
Formula:C13H11BCl2O3
InChI:InChI=1S/C13H11BCl2O3/c15-11-7-12(16)13(6-10(11)14(17)18)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
InChI key:InChIKey=WKVMHOHDMRUZMC-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=CC(B(O)O)=C(Cl)C=C2Cl
Synonyms:
  • (5-(Benzyloxy)-2,4-dichlorophenyl)boronicacid
  • [5-(Benzyloxy)-2,4-dichlorophenyl]boronic acid
  • Boronic acid, B-[2,4-dichloro-5-(phenylmethoxy)phenyl]-
  • B-[2,4-Dichloro-5-(phenylmethoxy)phenyl]boronic acid
  • 5-(Benzyloxy)-2,4-dichlorophenylboronic acid
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