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CAS 221006-68-4

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3,3-Dimethyl-6-oxocyclohex-1-enylboronic acid

Description:
3,3-Dimethyl-6-oxocyclohex-1-enylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic transformations, particularly in Suzuki coupling reactions. This compound features a cyclohexene ring with a ketone and two methyl substituents, contributing to its unique structural properties. The boronic acid moiety allows for the formation of stable complexes with diols and is pivotal in the development of pharmaceuticals and agrochemicals. Its molecular structure imparts specific steric and electronic properties, influencing its reactivity and interactions in chemical reactions. Additionally, the presence of the oxo group enhances its electrophilic character, making it a valuable intermediate in synthetic organic chemistry. The compound is typically handled with care due to the potential reactivity of the boronic acid group, and it may require specific storage conditions to maintain stability. Overall, 3,3-Dimethyl-6-oxocyclohex-1-enylboronic acid is a versatile building block in organic synthesis.
Formula:C8H13BO3
Synonyms:
  • Boronic acid, (3,3-dimethyl-6-oxo-1-cyclohexen-1-yl)- (9CI)
  • 3,3-Dimethyl-6-oxocyclohex-1-enylboronic acid
  • (3,3-DiMethyl-6-oxocyclohex-1-en-1-yl)boronic acid
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