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CAS 279262-35-0

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B-[4-(3-Methoxypropoxy)phenyl]boronic acid

Description:
B-[4-(3-Methoxypropoxy)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 3-methoxypropoxy group, enhancing its solubility and reactivity. Typically, boronic acids exhibit moderate to high polarity due to the presence of the boron atom and the acidic hydroxyl group, which can participate in hydrogen bonding. This compound may also exhibit unique properties such as the ability to act as a ligand in coordination chemistry or as a building block in the synthesis of more complex molecules. Its structural characteristics suggest potential applications in drug development, particularly in the design of inhibitors for certain biological targets. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C10H15BO4
InChI:InChI=1S/C10H15BO4/c1-14-7-2-8-15-10-5-3-9(4-6-10)11(12)13/h3-6,12-13H,2,7-8H2,1H3
InChI key:InChIKey=WYIXRPIOLPCEBP-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(OCCCOC)C=C1
Synonyms:
  • Boronic acid, [4-(3-methoxypropoxy)phenyl]-
  • B-[4-(3-Methoxypropoxy)phenyl]boronic acid
  • Boronic acid, B-[4-(3-methoxypropoxy)phenyl]-
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