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CAS 1946843-21-5

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B-[6-(Hydroxymethyl)-2-naphthalenyl]boronic acid

Description:
B-[6-(Hydroxymethyl)-2-naphthalenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene derivative. This compound features a hydroxymethyl group at the 6-position of the naphthalene ring, which enhances its solubility and reactivity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis, medicinal chemistry, and materials science. The presence of the naphthalene moiety contributes to its aromatic properties, potentially influencing its electronic characteristics and interactions with other molecules. This compound may exhibit unique properties such as fluorescence or photostability, depending on its structural context. Additionally, boronic acids are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds in organic synthesis. Overall, B-[6-(Hydroxymethyl)-2-naphthalenyl]boronic acid is a versatile compound with significant implications in chemical research and development.
Formula:C11H11BO3
InChI:InChI=1S/C11H11BO3/c13-7-8-1-2-10-6-11(12(14)15)4-3-9(10)5-8/h1-6,13-15H,7H2
InChI key:InChIKey=QDRGXVPUGZYLOR-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC2=C(C=C(CO)C=C2)C=C1
Synonyms:
  • B-[6-(Hydroxymethyl)-2-naphthalenyl]boronic acid
  • Boronic acid, B-[6-(hydroxymethyl)-2-naphthalenyl]-
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