CymitQuimica logo

CAS 747413-21-4

:

4-(4-Methyl-1-piperazinyl)benzeneboronic acid pinacol ester

Description:
4-(4-Methyl-1-piperazinyl)benzeneboronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is known for its ability to form reversible covalent bonds with diols and is often utilized in organic synthesis and medicinal chemistry. This compound features a piperazine ring, which contributes to its biological activity and solubility properties. The presence of the pinacol ester moiety enhances its stability and reactivity, making it suitable for various applications, including drug development and material science. The molecular structure includes a phenyl group substituted with a piperazine and a boronic acid derivative, which can participate in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the compound's properties, such as solubility, melting point, and reactivity, can be influenced by the presence of the methyl group on the piperazine, which may affect its steric and electronic characteristics. Overall, this compound is significant in the context of synthetic chemistry and potential pharmaceutical applications.
Formula:C17H27BN2O2
InChI:InChI=1/C17H27BN2O2/c1-16(2)17(3,4)22-18(21-16)14-6-8-15(9-7-14)20-12-10-19(5)11-13-20/h6-9H,10-13H2,1-5H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2)N2CCN(C)CC2)O1
Synonyms:
  • 1-Methyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperazine
  • Piperazine, 1-methyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.