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CAS 1021431-39-9

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B-[2-Formyl-5-methoxy-4-(phenylmethoxy)phenyl]boronic acid

Description:
B-[2-Formyl-5-methoxy-4-(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 substituent and a formyl group, contributing to its reactivity and potential as a building block in the synthesis of more complex molecules. The methoxy group enhances its solubility in organic solvents and may influence its electronic properties. Additionally, the presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a valuable method for forming carbon-carbon bonds. Overall, this compound's unique structural features and functional groups make it a versatile intermediate in organic synthesis and a subject of interest in the development of new materials and pharmaceuticals.
Formula:C15H15BO5
InChI:InChI=1S/C15H15BO5/c1-20-14-8-13(16(18)19)12(9-17)7-15(14)21-10-11-5-3-2-4-6-11/h2-9,18-19H,10H2,1H3
InChI key:InChIKey=VZSMEOPFMJZHCI-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(OC)C=C(B(O)O)C(C=O)=C2
Synonyms:
  • Boronic acid, B-[2-formyl-5-methoxy-4-(phenylmethoxy)phenyl]-
  • B-[2-Formyl-5-methoxy-4-(phenylmethoxy)phenyl]boronic acid
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