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CAS 154549-38-9

:

2,4,6-Triisopropylbenzeneboronic acid

Description:
2,4,6-Triisopropylbenzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a triisopropyl-substituted benzene ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and ethanol, while being less soluble in water due to its hydrophobic isopropyl groups. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. Its structure contributes to its unique reactivity, including the ability to form stable complexes with diols and other Lewis bases. Additionally, the steric bulk provided by the isopropyl groups can influence its reactivity and selectivity in chemical transformations. As with many organoboron compounds, it is important to handle this substance with care, as boronic acids can be sensitive to moisture and air, potentially affecting their stability and reactivity.
Formula:C15H25BO2
InChI:InChI=1/C15H25BO2/c1-9(2)12-7-13(10(3)4)15(16(17)18)14(8-12)11(5)6/h7-11,17-18H,1-6H3
SMILES:CC(C)c1cc(C(C)C)c(c(c1)C(C)C)B(O)O
Synonyms:
  • (2,4,6-Triisopropylphenyl)boronic acid
  • boronic acid, B-[2,4,6-tris(1-methylethyl)phenyl]-
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