CAS 913835-45-7
:[4-(2-morpholinoethylcarbamoyl)phenyl]boronic acid
Description:
[4-(2-Morpholinoethylcarbamoyl)phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amide functional group. This compound features a morpholinoethyl substituent, which contributes to its solubility and potential biological activity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including drug development and materials science. The presence of the morpholino group may enhance the compound's interaction with biological targets, potentially influencing its pharmacological properties. Additionally, the compound's structure suggests it may participate in Suzuki coupling reactions, a common method for synthesizing biaryl compounds in organic chemistry. Its unique characteristics, including its ability to act as a ligand in coordination chemistry and its potential use in medicinal chemistry, make it a subject of interest in research and development. Overall, [4-(2-morpholinoethylcarbamoyl)phenyl]boronic acid exemplifies the versatility of boronic acids in both synthetic and biological contexts.
Formula:C13H19BN2O4
InChI:InChI=1/C13H19BN2O4/c17-13(11-1-3-12(4-2-11)14(18)19)15-5-6-16-7-9-20-10-8-16/h1-4,18-19H,5-10H2,(H,15,17)
SMILES:c1cc(ccc1C(=O)NCCN1CCOCC1)B(O)O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
(4-((2-Morpholinoethyl)carbamoyl)phenyl)boronic acid
CAS:Formula:C13H19BN2O4Purity:98%Color and Shape:SolidMolecular weight:278.11204-[(2-Morpholin-4-ylethyl)carbamoyl]benzeneboronic acid
CAS:<p>4-[(2-Morpholin-4-ylethyl)carbamoyl]benzeneboronic acid</p>Formula:C13H19BN2O4Purity:98%Color and Shape: white solidMolecular weight:278.11g/mol(4-((2-Morpholinoethyl)carbamoyl)phenyl)boronic acid
CAS:Formula:C13H19BN2O4Purity:98%Molecular weight:278.12


