CymitQuimica logo

CAS 850411-14-2

:

4-[3-Ethoxycarbonyl-1-piperidinylcarbonyl]benzeneboronic acid pinacol ester

Description:
4-[3-Ethoxycarbonyl-1-piperidinylcarbonyl]benzeneboronic acid pinacol ester is a chemical compound characterized by its boronic acid ester functionality, which is significant in various organic synthesis applications, particularly in Suzuki coupling reactions. The presence of the piperidine ring contributes to its potential as a pharmacophore, enhancing its biological activity. The ethoxycarbonyl group introduces a carbonyl moiety that can participate in further chemical transformations, making the compound versatile in synthetic chemistry. The pinacol ester moiety provides stability and solubility, facilitating its use in various organic reactions. This compound is typically utilized in medicinal chemistry and material science due to its ability to form covalent bonds with diols and other nucleophiles. Its structural complexity allows for potential applications in drug development and the synthesis of complex organic molecules. As with many boronic acid derivatives, it is essential to handle this compound with care, considering its reactivity and the specific conditions required for its use in synthetic pathways.
Formula:C21H30BNO5
InChI:InChI=1/C21H30BNO5/c1-6-26-19(25)16-8-7-13-23(14-16)18(24)15-9-11-17(12-10-15)22-27-20(2,3)21(4,5)28-22/h9-12,16H,6-8,13-14H2,1-5H3
SMILES:CCOC(=O)C1CCCN(C1)C(=O)c1ccc(cc1)B1OC(C)(C)C(C)(C)O1
Synonyms:
  • Ethyl 1-{[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]Carbonyl}Piperidine-3-Carboxylate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.