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CAS 146862-02-4

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[4-(TRANS-4-N-PROPYLCYCLOHEXYL)PHENYL]BORONIC ACID

Description:
[4-(TRANS-4-N-PROPYLCYCLOHEXYL)PHENYL]BORONIC ACID, with the CAS number 146862-02-4, 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-propylcyclohexyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and materials science. The presence of the bulky propylcyclohexyl group can influence its solubility and steric properties, potentially enhancing its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, boronic acids are known for their role in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. The compound's structural features may also impart unique physical properties, such as melting point and boiling point, which are essential for its practical applications. Overall, [4-(TRANS-4-N-PROPYLCYCLOHEXYL)PHENYL]BORONIC ACID represents a versatile building block in synthetic organic chemistry.
Formula:C15H23BO2
InChI:InChI=1/C15H23BO2/c1-2-3-12-4-6-13(7-5-12)14-8-10-15(11-9-14)16(17)18/h8-13,17-18H,2-7H2,1H3/t12-,13-
SMILES:CCC[C@H]1CC[C@@H](CC1)c1ccc(cc1)B(O)O
Synonyms:
  • [4-(Trans-4-propylcyclohexyl)phenyl]-boronic acid
  • boronic acid, B-[4-(trans-4-propylcyclohexyl)phenyl]-
  • 4-(Trans-4-Propylcyclohexyl)Phenylboronic Acid
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