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CAS 141091-37-4

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Cyclohexene-1-boronic acid pinacol ester

Description:
Cyclohexene-1-boronic acid pinacol ester is an organoboron compound characterized by its boronic acid functionality, which is typically used in organic synthesis, particularly in Suzuki coupling reactions. This compound features a cyclohexene ring, which contributes to its reactivity and stability, and a pinacol ester group that enhances its solubility and handling properties. The presence of the boron atom allows for the formation of covalent bonds with various nucleophiles, making it a valuable intermediate in the synthesis of complex organic molecules. Cyclohexene-1-boronic acid pinacol ester is generally a colorless to pale yellow liquid, with a moderate boiling point and low volatility, which aids in its application in laboratory settings. It is important to handle this compound with care, as boronic acids can be sensitive to moisture and air, potentially leading to hydrolysis. Overall, its unique structure and reactivity make it a significant compound in the field of synthetic organic chemistry.
Formula:C12H21BO2
InChI:InChI=1/C12H21BO2/c1-11(2)12(3,4)15-13(14-11)10-8-6-5-7-9-10/h8H,5-7,9H2,1-4H3
SMILES:CC1(C)C(C)(C)OB(C2=CCCCC2)O1
Synonyms:
  • 2-Cyclohexenyl-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane
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