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CAS 833486-92-3

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[2-(2-methylpropoxy)phenyl]boronic acid

Description:
[2-(2-Methylpropoxy)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 2-methylpropoxy group, enhancing its solubility and reactivity. The boronic acid moiety contributes to its role in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the alkoxy group can influence the compound's electronic properties and sterics, affecting its reactivity and interaction with biological targets. The compound is typically a white to off-white solid and is soluble in polar organic solvents. Its applications extend to drug development, particularly in the design of inhibitors for certain enzymes, such as proteasomes, due to the boronic acid's ability to mimic natural substrates. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C10H15BO3
InChI:InChI=1/C10H15BO3/c1-8(2)7-14-10-6-4-3-5-9(10)11(12)13/h3-6,8,12-13H,7H2,1-2H3
SMILES:CC(C)COc1ccccc1B(O)O
Synonyms:
  • (2-Isobutoxyphenyl)boronic acid
  • boronic acid, B-[2-(2-methylpropoxy)phenyl]-
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