CymitQuimica logo

CAS 913835-41-3

:

[4-[benzyl(ethyl)carbamoyl]phenyl]boronic acid

Description:
[4-[Benzyl(ethyl)carbamoyl]phenyl]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, making it useful in various applications, including drug development and materials science. The compound features a phenyl ring substituted with a benzyl group and an ethyl carbamoyl moiety, contributing to its structural complexity and potential biological activity. Boronic acids are often utilized in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. The presence of the carbamoyl group may enhance the compound's solubility and reactivity, while the benzyl substituent can influence its interaction with biological targets. Overall, this compound's unique structure suggests potential applications in medicinal chemistry, particularly in the development of inhibitors or modulators of biological pathways. Its specific properties, such as solubility, stability, and reactivity, would depend on the surrounding conditions and the presence of other functional groups in a given reaction or application.
Formula:C16H18BNO3
InChI:InChI=1/C16H18BNO3/c1-2-18(12-13-6-4-3-5-7-13)16(19)14-8-10-15(11-9-14)17(20)21/h3-11,20-21H,2,12H2,1H3
SMILES:CCN(Cc1ccccc1)C(=O)c1ccc(cc1)B(O)O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.