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CAS 876189-18-3

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(5-methoxycarbonyl-2-methyl-phenyl)boronic acid

Description:
(5-Methoxycarbonyl-2-methyl-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a methoxycarbonyl group and a methyl group, contributing to its unique reactivity and solubility properties. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the presence of the methoxycarbonyl group enhances its stability and solubility in organic solvents. The compound's structure suggests potential applications in drug development and materials science, particularly in the synthesis of complex organic molecules. Its specific reactivity and interactions can be influenced by the electronic effects of the substituents on the phenyl ring, making it a valuable compound for research in synthetic organic chemistry.
Formula:C9H11BO4
InChI:InChI=1/C9H11BO4/c1-6-3-4-7(9(11)14-2)5-8(6)10(12)13/h3-5,12-13H,1-2H3
SMILES:Cc1ccc(cc1B(O)O)C(=O)OC
Synonyms:
  • [5-(Methoxycarbonyl)-2-methylphenyl]boronic acid
  • Benzoic Acid, 3-Borono-4-Methyl-, Methyl Ester
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