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CAS 871126-26-0

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B-[3-[[4-(2-Methoxyethyl)phenoxy]methyl]phenyl]boronic acid

Description:
B-[3-[[4-(2-Methoxyethyl)phenoxy]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 methoxyethyl group, enhancing its solubility and reactivity. The boronic acid moiety is crucial for applications in medicinal chemistry, particularly in drug design and development, as it can participate in various chemical reactions, including Suzuki coupling, which is essential for synthesizing complex organic molecules. Additionally, the compound may exhibit properties such as moderate to high polarity due to the presence of the methoxyethyl group and the boronic acid, influencing its interactions in biological systems. Its structural characteristics suggest potential utility in targeting specific biological pathways, making it a candidate for further research in therapeutic applications. As with many organoboron compounds, careful handling and storage are necessary due to their sensitivity to moisture and air.
Formula:C16H19BO4
InChI:InChI=1S/C16H19BO4/c1-20-10-9-13-5-7-16(8-6-13)21-12-14-3-2-4-15(11-14)17(18)19/h2-8,11,18-19H,9-10,12H2,1H3
InChI key:InChIKey=RABCYEGFKLWONK-UHFFFAOYSA-N
SMILES:C(OC1=CC=C(CCOC)C=C1)C2=CC(B(O)O)=CC=C2
Synonyms:
  • Boronic acid, B-[3-[[4-(2-methoxyethyl)phenoxy]methyl]phenyl]-
  • [3-[4-(2-Methoxyethyl)phenoxymethyl]phenyl]boronic acid
  • B-[3-[[4-(2-Methoxyethyl)phenoxy]methyl]phenyl]boronic acid
  • Boronic acid, [3-[[4-(2-methoxyethyl)phenoxy]methyl]phenyl]-
  • (3-((4-(2-Methoxyethyl)phenoxy)methyl)phenyl)boronic acid
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