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CAS 143651-26-7

:

[4-(trans-4-pentylcyclohexyl)phenyl]boronic acid

Description:
[4-(trans-4-pentylcyclohexyl)phenyl]boronic acid, with the CAS number 143651-26-7, 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-pentylcyclohexyl group. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity due to the boronic acid moiety, which can participate in various chemical reactions, including Suzuki coupling. The presence of the pentylcyclohexyl group contributes to its hydrophobic characteristics, influencing its interactions in biological and chemical systems. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in sensor applications and organic synthesis. The compound's structural features may also impart unique thermal and optical properties, making it of interest in materials science, particularly in the development of liquid crystal displays and other electronic materials.
Formula:C17H27BO2
InChI:InChI=1/C17H27BO2/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(13-11-16)18(19)20/h10-15,19-20H,2-9H2,1H3/t14-,15-
SMILES:CCCCC[C@H]1CC[C@@H](CC1)c1ccc(cc1)B(O)O
Synonyms:
  • 4-(Trans-4-pentylcyclohexyl)phenyl]-boronic acid
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