CAS 1310384-30-5
:B-(2-Ethoxy-6-methyl-3-pyridinyl)boronic acid
Description:
B-(2-Ethoxy-6-methyl-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically exhibits properties such as moderate solubility in polar organic solvents due to the ethoxy group, which enhances its hydrophilicity. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and organic synthesis. The presence of the methyl and ethoxy substituents on the pyridine ring can influence its reactivity and interaction with biological targets. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Overall, B-(2-Ethoxy-6-methyl-3-pyridinyl)boronic acid is a versatile compound with potential applications in drug development and materials science, owing to its unique structural features and reactivity.
Formula:C8H12BNO3
InChI:InChI=1S/C8H12BNO3/c1-3-13-8-7(9(11)12)5-4-6(2)10-8/h4-5,11-12H,3H2,1-2H3
InChI key:InChIKey=UOAWUEZHOQVXBO-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC)N=C(C)C=C1
Synonyms:- Boronic acid, B-(2-ethoxy-6-methyl-3-pyridinyl)-
- B-(2-Ethoxy-6-methyl-3-pyridinyl)boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
