CymitQuimica logo

CAS 870779-00-3

:

(4-{[4-(2-methoxyethyl)phenoxy]methyl}phenyl)boronic acid

Description:
(4-{[4-(2-methoxyethyl)phenoxy]methyl}phenyl)boronic acid, with the CAS number 870779-00-3, 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. This compound features a phenyl ring substituted with a methoxyethyl group and a phenoxy group, contributing to its potential applications in medicinal chemistry and materials science. The boronic acid moiety allows for interactions with biological molecules, making it useful in drug development and as a tool in biochemical research. Its solubility in organic solvents and moderate polarity can facilitate its use in various chemical reactions, including Suzuki coupling reactions, which are pivotal in the synthesis of complex organic molecules. The presence of the methoxyethyl group may enhance its solubility and stability, while the overall structure suggests potential for selective binding and reactivity, making it a compound of interest in both synthetic and applied chemistry contexts.
Formula:C16H19BO4
InChI:InChI=1/C16H19BO4/c1-20-11-10-13-4-8-16(9-5-13)21-12-14-2-6-15(7-3-14)17(18)19/h2-9,18-19H,10-12H2,1H3
SMILES:COCCc1ccc(cc1)OCc1ccc(cc1)B(O)O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.