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CAS 957062-62-3

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B-[4-(2-Nitrophenoxy)phenyl]boronic acid

Description:
B-[4-(2-Nitrophenoxy)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 2-nitrophenoxy group, which introduces both electron-withdrawing and steric effects that can influence its reactivity and solubility. Typically, boronic acids exhibit moderate solubility in polar solvents, and their reactivity can be modulated by the substituents on the aromatic rings. This specific compound may also exhibit properties such as fluorescence or photostability, depending on its molecular structure. 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-[4-(2-Nitrophenoxy)phenyl]boronic acid is a versatile compound with potential applications in drug development and materials science.
Formula:C12H10BNO5
InChI:InChI=1S/C12H10BNO5/c15-13(16)9-5-7-10(8-6-9)19-12-4-2-1-3-11(12)14(17)18/h1-8,15-16H
InChI key:InChIKey=COFSQPXQXYCXFW-UHFFFAOYSA-N
SMILES:O(C1=C(N(=O)=O)C=CC=C1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • B-[4-(2-Nitrophenoxy)phenyl]boronic acid
  • Boronic acid, B-[4-(2-nitrophenoxy)phenyl]-
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