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CAS 847861-96-5

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B-[5-(Dimethylamino)-1-naphthalenyl]boronic acid

Description:
B-[5-(Dimethylamino)-1-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 dimethylamino group, which enhances its solubility and reactivity. Typically, boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the naphthalene moiety contributes to its aromatic properties, potentially influencing its electronic characteristics and reactivity. This compound may also exhibit fluorescence, which can be useful in biological imaging or sensing applications. Additionally, due to the boronic acid functionality, it can participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Overall, B-[5-(Dimethylamino)-1-naphthalenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry and materials science.
Formula:C12H14BNO2
InChI:InChI=1S/C12H14BNO2/c1-14(2)12-8-4-5-9-10(12)6-3-7-11(9)13(15)16/h3-8,15-16H,1-2H3
InChI key:InChIKey=SAYNXCVNUHTVEG-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2=C(C(N(C)C)=CC=C2)C=CC1
Synonyms:
  • Boronic acid, [5-(dimethylamino)-1-naphthalenyl]-
  • B-[5-(Dimethylamino)-1-naphthalenyl]boronic acid
  • [5-(Dimethylamino)naphthalen-1-yl]boronic acid
  • Boronic acid, B-[5-(dimethylamino)-1-naphthalenyl]-
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