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CAS 1256346-32-3

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B-[4-(trans-4-Propylcyclohexyl)-1-cyclohexen-1-yl]boronic acid

Description:
B-[4-(trans-4-Propylcyclohexyl)-1-cyclohexen-1-yl]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 reactions, particularly in Suzuki coupling reactions. The structure features a cyclohexene ring substituted with a propylcyclohexyl group, contributing to its hydrophobic characteristics and potentially influencing its solubility in organic solvents. The boronic acid moiety imparts acidity, allowing it to participate in acid-base reactions. This compound may exhibit interesting properties such as selective reactivity and potential applications in organic synthesis, medicinal chemistry, and materials science. Its unique structural features could also lead to specific interactions in biological systems, making it a candidate for further research in drug development or as a molecular probe. As with many boronic acids, stability in aqueous environments and sensitivity to moisture are important considerations for handling and storage.
Formula:C15H27BO2
InChI:InChI=1/C15H27BO2/c1-2-3-12-4-6-13(7-5-12)14-8-10-15(11-9-14)16(17)18/h10,12-14,17-18H,2-9,11H2,1H3/t12-,13-,14?
InChI key:InChIKey=ZDOBCKIGBGWTHO-QSPIWVMWNA-N
SMILES:B(O)(O)C=1CC[C@](CC1)([C@@H]2CC[C@@H](CCC)CC2)[H]
Synonyms:
  • B-[4-(trans-4-Propylcyclohexyl)-1-cyclohexen-1-yl]boronic acid
  • Boronic acid, B-[4-(trans-4-propylcyclohexyl)-1-cyclohexen-1-yl]-
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