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CAS 1256358-61-8

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B-[3-[(2-Methoxyethoxy)methyl]phenyl]boronic acid

Description:
B-[3-[(2-Methoxyethoxy)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. This compound features a phenyl ring substituted with a methoxyethoxy group, enhancing its solubility and reactivity. The boronic acid moiety allows for applications in organic synthesis, particularly in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, the presence of the methoxyethoxy group may contribute to its hydrophilicity, making it suitable for various biological and chemical applications. The compound's structure suggests potential uses in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its unique properties, including the ability to participate in complexation and its role in drug delivery systems, make it a valuable substance in both research and industrial applications. As with many boronic acids, care must be taken in handling due to their sensitivity to moisture and air.
Formula:C10H15BO4
InChI:InChI=1S/C10H15BO4/c1-14-5-6-15-8-9-3-2-4-10(7-9)11(12)13/h2-4,7,12-13H,5-6,8H2,1H3
InChI key:InChIKey=SDOBFXINMOTWOZ-UHFFFAOYSA-N
SMILES:C(OCCOC)C1=CC(B(O)O)=CC=C1
Synonyms:
  • 3-[(2-Methoxyethoxy)methyl]phenylboronic acid
  • (3-((2-Methoxyethoxy)methyl)phenyl)boronicacid
  • [3-[(2-Methoxyethoxy)methyl]phenyl]boronic acid
  • Boronic acid, B-[3-[(2-methoxyethoxy)methyl]phenyl]-
  • B-[3-[(2-Methoxyethoxy)methyl]phenyl]boronic acid
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