CAS 1451391-64-2
:B-(2-Methyl-5-propoxyphenyl)boronic acid
Description:
B-(2-Methyl-5-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a propoxy group and a methyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the propoxy and methyl substituents can influence its solubility, reactivity, and interaction with biological targets. Boronic acids are known for their role in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis. Additionally, the specific structural features of B-(2-Methyl-5-propoxyphenyl)boronic acid may impart unique properties that can be exploited in drug development or materials science. Overall, this compound represents a versatile building block in synthetic chemistry, with potential applications in pharmaceuticals and advanced materials.
Formula:C10H15BO3
InChI:InChI=1S/C10H15BO3/c1-3-6-14-9-5-4-8(2)10(7-9)11(12)13/h4-5,7,12-13H,3,6H2,1-2H3
InChI key:InChIKey=PIGHFUHZRWCYCY-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(OCCC)=CC=C1C
Synonyms:- Boronic acid, B-(2-methyl-5-propoxyphenyl)-
- B-(2-Methyl-5-propoxyphenyl)boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
