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CAS 164220-57-9

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B-[4-(trans-4-Ethylcyclohexyl)phenyl]boronic acid

Description:
B-[4-(trans-4-Ethylcyclohexyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a trans-4-ethylcyclohexyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the ethylcyclohexyl substituent can influence its solubility, stability, and reactivity, potentially enhancing its lipophilicity compared to simpler boronic acids. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's specific characteristics, such as melting point, boiling point, and solubility, would depend on its molecular structure and the interactions of its functional groups with solvents and other reagents. Overall, B-[4-(trans-4-Ethylcyclohexyl)phenyl]boronic acid is a valuable compound in the field of organic chemistry.
Formula:C14H21BO2
InChI:InChI=1/C14H21BO2/c1-2-11-3-5-12(6-4-11)13-7-9-14(10-8-13)15(16)17/h7-12,16-17H,2-6H2,1H3/t11-,12-
InChI key:InChIKey=QRCCELWUDZLZLP-HAQNSBGRNA-N
SMILES:B(O)(O)C1=CC=C(C=C1)[C@H]2CC[C@H](CC)CC2
Synonyms:
  • Boronic acid, B-[4-(trans-4-ethylcyclohexyl)phenyl]-
  • Boronic acid, [4-(4-ethylcyclohexyl)phenyl]-, trans-
  • B-[4-(trans-4-Ethylcyclohexyl)phenyl]boronic acid
  • 4-(trans-4-Ethylcyclohexyl)phenylboronic acid
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