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CAS 1627917-17-2

:

B-Benzo[b]naphtho[2,3-d]furan-2-ylboronic acid

Description:
B-Benzo[b]naphtho[2,3-d]furan-2-ylboronic acid is an organic 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 reactions, particularly in Suzuki coupling reactions. This compound features a complex polycyclic structure that includes a fused naphthalene and furan moiety, contributing to its unique chemical properties and potential applications in organic synthesis and materials science. The boronic acid group enhances its reactivity and solubility in polar solvents, facilitating its use in medicinal chemistry and the development of boron-containing materials. Additionally, compounds like this one are often studied for their potential biological activities, including anti-cancer properties, due to their ability to interact with biological molecules. Overall, B-Benzo[b]naphtho[2,3-d]furan-2-ylboronic acid exemplifies the intersection of organic chemistry and materials science, showcasing the versatility of boron-containing compounds in various applications.
Formula:C16H11BO3
InChI:InChI=1S/C16H11BO3/c18-17(19)12-5-6-15-14(9-12)13-7-10-3-1-2-4-11(10)8-16(13)20-15/h1-9,18-19H
InChI key:InChIKey=FGXHNQHUZOHBRS-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C2C=3C(OC2=CC1)=CC=4C(C3)=CC=CC4
Synonyms:
  • Boronic acid, B-benzo[b]naphtho[2,3-d]furan-2-yl-
  • B-Benzo[b]naphtho[2,3-d]furan-2-ylboronic acid
  • Benzo[b]naphtho[2,3-d]furan-2-boronic acid
  • Naphtho[2,3-b]benzofuran-2-ylboronic acid
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