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CAS 850567-91-8

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B-[4-(1,1-Dimethylethyl)-1-cyclohexen-1-yl]boronic acid

Description:
B-[4-(1,1-Dimethylethyl)-1-cyclohexen-1-yl]boronic acid, with the CAS number 850567-91-8, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a cyclohexene ring. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar solvents like water and alcohols due to the boronic acid moiety. The presence of the bulky tert-butyl group enhances its steric properties, which can influence its reactivity and interactions in various chemical reactions, particularly in Suzuki coupling reactions, where it serves as a key intermediate in the formation of carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. The compound's stability and reactivity can be affected by environmental factors such as pH and temperature, which are important considerations in its handling and application in synthetic chemistry.
Formula:C10H19BO2
InChI:InChI=1S/C10H19BO2/c1-10(2,3)8-4-6-9(7-5-8)11(12)13/h6,8,12-13H,4-5,7H2,1-3H3
InChI key:InChIKey=QPJWLDFYBBQYSG-UHFFFAOYSA-N
SMILES:C(C)(C)(C)C1CCC(B(O)O)=CC1
Synonyms:
  • (4-(tert-Butyl)cyclohex-1-en-1-yl)boronic acid
  • (4-(tert-Butyl)cyclohex-1-en-1-yl)boronicacid
  • (4-Tert-Butylcyclohexen-1-Yl)Boronic Acid
  • (4-tert-Butylcyclohex-1-en-1-yl)boronic acid
  • B-[4-(1,1-Dimethylethyl)-1-cyclohexen-1-yl]boronic acid
  • Boronic acid, [4-(1,1-dimethylethyl)-1-cyclohexen-1-yl]-
  • boronic acid, B-[4-(1,1-dimethylethyl)-1-cyclohexen-1-yl]-
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