CAS 290348-01-5
:B-[4-Methoxy-3-(1-methylethyl)phenyl]boronic acid
Description:
B-[4-Methoxy-3-(1-methylethyl)phenyl]boronic acid is an organoboron 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 methoxy group and an isopropyl group, contributing to its hydrophobic characteristics and potential reactivity in various chemical reactions, particularly in Suzuki coupling reactions. The boronic acid moiety allows for the formation of complexes with biomolecules, making it useful in medicinal chemistry and materials science. Its solubility in organic solvents and moderate stability under standard conditions are notable characteristics. Additionally, the compound may exhibit specific biological activities, which can be explored in pharmaceutical applications. As with many boronic acids, it is essential to handle this compound with care due to its potential reactivity and the need for proper storage conditions to maintain its integrity.
Formula:C10H15BO3
InChI:InChI=1S/C10H15BO3/c1-7(2)9-6-8(11(12)13)4-5-10(9)14-3/h4-7,12-13H,1-3H3
InChI key:InChIKey=ILKURCOQRCUYRU-UHFFFAOYSA-N
SMILES:C(C)(C)C1=C(OC)C=CC(B(O)O)=C1
Synonyms:- [4-Methoxy-3-(propan-2-yl)phenyl]boronic acid
- Boronic acid, B-[4-methoxy-3-(1-methylethyl)phenyl]-
- B-[4-Methoxy-3-(1-methylethyl)phenyl]boronic acid
- Boronic acid, [4-methoxy-3-(1-methylethyl)phenyl]-
- (3-Isopropyl-4-methoxyphenyl)boronic acid
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