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CAS 1256345-76-2

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B-[3-Methyl-5-(1-methylethoxy)phenyl]boronic acid

Description:
B-[3-Methyl-5-(1-methylethoxy)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, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a methyl group and an isopropoxy group, contributing to its hydrophobic properties and influencing its reactivity. Boronic acids are typically polar, allowing for solubility in polar solvents, while the presence of the bulky isopropoxy group may affect steric hindrance and reactivity. This compound can participate in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in the synthesis of complex organic molecules. Additionally, boronic acids have potential applications in drug development, particularly in the design of inhibitors for various biological targets. Overall, B-[3-Methyl-5-(1-methylethoxy)phenyl]boronic acid exemplifies the versatility of boron-containing compounds in synthetic chemistry.
Formula:C10H15BO3
InChI:InChI=1S/C10H15BO3/c1-7(2)14-10-5-8(3)4-9(6-10)11(12)13/h4-7,12-13H,1-3H3
InChI key:InChIKey=CZCHMHUSIRMAFN-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=CC(B(O)O)=CC(C)=C1
Synonyms:
  • Boronic acid, B-[3-methyl-5-(1-methylethoxy)phenyl]-
  • (3-Isopropoxy-5-methylphenyl)boronic acid
  • [3-Methyl-5-(propan-2-yloxy)phenyl]boronic acid
  • 3-Isopropoxy-5-methylphenylboronic acid
  • B-[3-Methyl-5-(1-methylethoxy)phenyl]boronic acid
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