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CAS 1398331-98-0

:

1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutanol

Description:
1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutanol is a chemical compound characterized by its unique structure, which includes a cyclobutanol moiety and a boron-containing dioxaborolane group. The presence of the cyclobutanol structure contributes to its potential as a chiral building block in organic synthesis, while the dioxaborolane group enhances its reactivity and solubility in various organic solvents. This compound is likely to exhibit interesting properties such as moderate polarity and the ability to participate in various chemical reactions, including cross-coupling reactions, due to the boron atom's electrophilic nature. Additionally, the bulky tetramethyl groups provide steric hindrance, which can influence the compound's reactivity and stability. Its applications may extend to medicinal chemistry, materials science, and catalysis, where such structural features can be advantageous. Overall, this compound represents a versatile intermediate in synthetic organic chemistry, with potential implications in the development of new materials and pharmaceuticals.
Formula:C16H23BO3
InChI:InChI=1S/C16H23BO3/c1-14(2)15(3,4)20-17(19-14)13-8-6-12(7-9-13)16(18)10-5-11-16/h6-9,18H,5,10-11H2,1-4H3
InChI key:InChIKey=ADJDMTWSQDLRRP-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(C=C2)C3(O)CCC3
Synonyms:
  • 1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutanol
  • Cyclobutanol, 1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
  • 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutanol
  • (4-(1-HYDROXYCYCLOBUTYL)PHENYL)BORONIC ACID PINACOL ESTER
  • 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutan-1-ol
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