CymitQuimica logo

CAS 850567-28-1

:

[3-[(3-ethoxy-3-oxo-propyl)carbamoyl]phenyl]boronic acid

Description:
[3-[(3-ethoxy-3-oxo-propyl)carbamoyl]phenyl]boronic acid, with the CAS number 850567-28-1, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a carbamoyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The ethoxy and oxo groups contribute to its solubility and reactivity, enhancing its potential as a building block in drug development or as a ligand in catalysis. Additionally, boronic acids are known for their role in the Suzuki coupling reaction, a key method for forming carbon-carbon bonds. The compound's structure suggests it may also exhibit biological activity, potentially interacting with specific biological targets. Overall, this substance is of interest in both synthetic and pharmaceutical chemistry due to its unique functional groups and reactivity.
Formula:C12H16BNO5
InChI:InChI=1/C12H16BNO5/c1-2-19-11(15)6-7-14-12(16)9-4-3-5-10(8-9)13(17)18/h3-5,8,17-18H,2,6-7H2,1H3,(H,14,16)
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.