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CAS 193905-93-0

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(3-t-Butyl-5-methylphenyl)boronic acid

Description:
(3-t-Butyl-5-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. This compound features a bulky t-butyl group and a methyl group on the aromatic ring, which can influence its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The presence of the t-butyl group enhances steric hindrance, which can affect the compound's reactivity and selectivity in chemical reactions. Additionally, the boronic acid group can participate in various transformations, including the formation of boronate esters. This compound is typically used in research and development, particularly in the synthesis of complex organic molecules and in materials science. Its properties, such as solubility and stability, can vary depending on the solvent and conditions used in reactions.
Formula:C11H17BO2
InChI:InChI=1/C11H17BO2/c1-8-5-9(11(2,3)4)7-10(6-8)12(13)14/h5-7,13-14H,1-4H3
SMILES:Cc1cc(cc(c1)B(O)O)C(C)(C)C
Synonyms:
  • (3-Tert-Butyl-5-Methylphenyl)Boronic Acid
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