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CAS 1217500-82-7

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B-[2-[(Dimethylamino)methyl]-5-nitrophenyl]boronic acid

Description:
B-[2-[(Dimethylamino)methyl]-5-nitrophenyl]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 and other nucleophiles. This compound features a nitrophenyl moiety, which contributes to its electronic properties and potential reactivity. The dimethylamino group enhances its solubility and may influence its biological activity, making it of interest in medicinal chemistry and materials science. Typically, boronic acids are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. The presence of the nitro group can also impart unique optical properties and reactivity patterns. Additionally, the compound may exhibit pH-dependent behavior due to the acidic nature of the boronic acid group, which can affect its stability and reactivity in various environments. Overall, this compound's structural features suggest potential applications in drug development and as a building block in organic synthesis.
Formula:C9H13BN2O4
InChI:InChI=1S/C9H13BN2O4/c1-11(2)6-7-3-4-8(12(15)16)5-9(7)10(13)14/h3-5,13-14H,6H2,1-2H3
InChI key:InChIKey=MMPDPMGUOBVIPN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(CN(C)C)C=CC(N(=O)=O)=C1
Synonyms:
  • Boronic acid, B-[2-[(dimethylamino)methyl]-5-nitrophenyl]-
  • B-[2-[(Dimethylamino)methyl]-5-nitrophenyl]boronic acid
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