CAS 1451391-98-2
:B-(2-Methoxy-3,5-dimethylphenyl)boronic acid
Description:
B-(2-Methoxy-3,5-dimethylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. This compound features a methoxy group and two methyl groups on the aromatic ring, which contribute to its unique chemical properties. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the methoxy and methyl substituents can influence the compound's solubility, reactivity, and interaction with biological targets. Typically, boronic acids are utilized in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the specific structure of B-(2-Methoxy-3,5-dimethylphenyl)boronic acid may impart distinct electronic and steric properties, affecting its behavior in chemical reactions and potential applications in drug development and materials science.
Formula:C9H13BO3
InChI:InChI=1S/C9H13BO3/c1-6-4-7(2)9(13-3)8(5-6)10(11)12/h4-5,11-12H,1-3H3
InChI key:InChIKey=UHTQRLCDAMYQFY-UHFFFAOYSA-N
SMILES:O(C)C1=C(B(O)O)C=C(C)C=C1C
Synonyms:- Boronic acid, B-(2-methoxy-3,5-dimethylphenyl)-
- B-(2-Methoxy-3,5-dimethylphenyl)boronic acid
- 3,5-Dimethyl-2-methoxyphenylboronic acid
- (2-Methoxy-3,5-dimethyl-phenyl)boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
