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CAS 854616-69-6

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B-[3-[(2-Propen-1-yloxy)methyl]phenyl]boronic acid

Description:
B-[3-[(2-Propen-1-yloxy)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. The compound features a phenyl ring substituted with a propenyloxy group, which enhances its reactivity and solubility in organic solvents. Boronic acids like this one are often employed in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the presence of the boron atom allows for potential applications in drug development, particularly in the design of inhibitors for certain enzymes. The compound's structure suggests it may exhibit interesting electronic properties and reactivity patterns, making it a valuable candidate for further research in materials science and pharmaceuticals. As with many boronic acids, it is important to handle this compound with care due to its sensitivity to moisture and air, which can affect its stability and reactivity.
Formula:C10H13BO3
InChI:InChI=1S/C10H13BO3/c1-2-6-14-8-9-4-3-5-10(7-9)11(12)13/h2-5,7,12-13H,1,6,8H2
InChI key:InChIKey=AURXILXTQYNTJO-UHFFFAOYSA-N
SMILES:C(OCC=C)C1=CC(B(O)O)=CC=C1
Synonyms:
  • Boronic acid, [3-[(2-propenyloxy)methyl]phenyl]-
  • B-[3-[(2-Propen-1-yloxy)methyl]phenyl]boronic acid
  • Boronic acid, B-[3-[(2-propen-1-yloxy)methyl]phenyl]-
  • [3-[(Allyloxy)methyl]phenyl]boronic acid
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