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CAS 4441-56-9

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B-Cyclohexylboronic acid

Description:
B-Cyclohexylboronic acid, with the CAS number 4441-56-9, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a cyclohexyl ring. This compound typically appears as a white to off-white solid and is known for its solubility in polar organic solvents, such as ethanol and methanol, while being less soluble in non-polar solvents. B-Cyclohexylboronic acid is notable for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Additionally, it serves as a building block in the synthesis of pharmaceuticals and agrochemicals. The compound exhibits typical boronic acid reactivity, including the ability to undergo oxidation and participate in Suzuki-Miyaura coupling reactions. Its stability and reactivity can be influenced by factors such as pH and the presence of other functional groups in a reaction mixture.
Formula:C6H13BO2
InChI:InChI=1S/C6H13BO2/c8-7(9)6-4-2-1-3-5-6/h6,8-9H,1-5H2
InChI key:InChIKey=XDRVAZAFNWDVOE-UHFFFAOYSA-N
SMILES:B(O)(O)C1CCCCC1
Synonyms:
  • B-Cyclohexylboronic acid
  • Boronic acid, B-cyclohexyl-
  • Boronic acid, cyclohexyl-
  • Boronic acid, cyclohexyl- (9CI)
  • Boronicacid, B-cyclohexyl-
  • Brn 1921820
  • Cyclohexaneboronic acid
  • Cyclohexylboric acid
  • 4-16-00-01653 (Beilstein Handbook Reference)
  • Cyclohexylboronic acid
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