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CAS 1256346-33-4

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

Description:
B-[4-(trans-4-Pentylcyclohexyl)-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 applications, including organic synthesis and materials science. The structure features a cyclohexenyl moiety substituted with a pentylcyclohexyl group, contributing to its hydrophobic characteristics and potential utility in liquid crystal applications. The compound's boronic acid group can participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is valuable in the synthesis of complex organic molecules. Additionally, its unique structural features may impart specific optical or electronic properties, making it of interest in the development of advanced materials. The compound is typically handled with care due to the reactivity of boronic acids, particularly in the presence of moisture, which can lead to hydrolysis. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and materials development.
Formula:C17H31BO2
InChI:InChI=1/C17H31BO2/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(13-11-16)18(19)20/h12,14-16,19-20H,2-11,13H2,1H3/t14-,15-,16?
InChI key:InChIKey=NSKYCIWGCMDXSO-MRJYIUEKNA-N
SMILES:C(CCCC)[C@@H]1CC[C@H](CC1)C2(CCC(B(O)O)=CC2)[H]
Synonyms:
  • B-[4-(trans-4-Pentylcyclohexyl)-1-cyclohexen-1-yl]boronic acid
  • Boronic acid, B-[4-(trans-4-pentylcyclohexyl)-1-cyclohexen-1-yl]-
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