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CAS 871329-72-5

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(4-ethylcyclohexen-1-yl)boronic acid

Description:
(4-Ethylcyclohexen-1-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a cyclohexene ring with an ethyl substituent. This compound typically exhibits a molecular structure that includes a six-membered carbon ring with a double bond, contributing to its reactivity and potential applications in organic synthesis. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical reactions, including Suzuki coupling reactions, which are essential in the formation of carbon-carbon bonds. Additionally, the presence of the ethyl group can influence the sterics and electronics of the molecule, potentially enhancing its reactivity or selectivity in chemical processes. (4-Ethylcyclohexen-1-yl)boronic acid is often utilized in medicinal chemistry and materials science, where its unique properties can be harnessed for the development of new pharmaceuticals or functional materials. As with many boronic acids, it may also exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions.
Formula:C8H15BO2
InChI:InChI=1/C8H15BO2/c1-2-7-3-5-8(6-4-7)9(10)11/h5,7,10-11H,2-4,6H2,1H3
SMILES:CCC1CC=C(CC1)B(O)O
Synonyms:
  • (4-Ethylcyclohex-1-en-1-yl)boronic acid
  • boronic acid, B-(4-ethyl-1-cyclohexen-1-yl)-
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