CymitQuimica logo

CAS 850568-57-9

:

[4-(2-methylpropyl)-3-nitrophenyl]boronic acid

Description:
[4-(2-Methylpropyl)-3-nitrophenyl]boronic acid is an organic 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 nitro group and a branched alkyl chain, specifically a 2-methylpropyl group, which contributes to its hydrophobic characteristics. The presence of the nitro group introduces electron-withdrawing properties, influencing the compound's reactivity and polarity. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. Additionally, this compound may exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its solubility and stability can vary depending on the solvent and pH conditions, making it important to consider these factors in practical applications. Overall, [4-(2-methylpropyl)-3-nitrophenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C10H14BNO4
InChI:InChI=1/C10H14BNO4/c1-7(2)5-8-3-4-9(11(13)14)6-10(8)12(15)16/h3-4,6-7,13-14H,5H2,1-2H3
SMILES:CC(C)Cc1ccc(cc1N(=O)=O)B(O)O
Synonyms:
  • (4-Isobutyl-3-nitrophenyl)boronic acid
  • boronic acid, B-[4-(2-methylpropyl)-3-nitrophenyl]-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.