logo
Home  > Chemistry  > Organometallic Reagents  > Organoboron  > 3-(4-Methoxybenzyloxy)phenylboronic acid

AD79400

1072951-89-3 | 3-(4-Methoxybenzyloxy)phenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
1g 96% in stock $58.00 $41.00 -   +
5g 96% in stock $187.00 $131.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD79400
Chemical Name: 3-(4-Methoxybenzyloxy)phenylboronic acid
CAS Number: 1072951-89-3
Molecular Formula: C14H15BO4
Molecular Weight: 258.0775
MDL Number: MFCD09038416
SMILES: COc1ccc(cc1)COc1cccc(c1)B(O)O

 

Computed Properties
Complexity: 254  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 5  

 

 

Upstream Synthesis Route
  • The compound (3-((4-Methoxybenzyl)oxy)phenyl)boronic acid is a versatile chemical reagent commonly used in organic synthesis. It is known for its ability to participate in a variety of reactions, making it a valuable tool for chemists working in the field of medicinal chemistry, materials science, and pharmaceuticals.One key application of this compound is in Suzuki-Miyaura cross-coupling reactions, where it serves as a boronate ester partner. This reaction allows for the formation of carbon-carbon bonds between an aryl halide or pseudohalide and an organoboron compound, resulting in the synthesis of biaryl compounds. The (3-((4-Methoxybenzyl)oxy)phenyl)boronic acid is particularly useful in this context due to its stability and compatibility with a wide range of functional groups.Additionally, this compound can be employed in the formation of functionalized phenols through borylation reactions. By reacting with aryl halides or pseudohalides in the presence of palladium catalysts, it can lead to the introduction of boronic ester moieties onto phenyl rings, enabling further derivatization and functionalization of the compounds.Overall, the (3-((4-Methoxybenzyl)oxy)phenyl)boronic acid plays a crucial role in modern synthetic chemistry by enabling the construction of complex molecular structures with precision and efficiency. Its versatility and robustness make it a valuable reagent for chemists striving to develop new molecules with diverse applications.
FEATURED PRODUCTS