5-Methyl-4-propoxy-1,3-phenylenebisboronic acid is a boronic acid derivative characterized by its unique structure, which includes two boronic acid functional groups attached to a phenylene backbone. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the methyl and propoxy substituents can influence its solubility, reactivity, and interaction with biological targets. Generally, boronic acids are known for their role in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, this compound may exhibit potential in drug development, particularly in targeting specific biomolecules due to its ability to interact with hydroxyl-containing compounds. Its stability, reactivity, and functionalization potential make it a valuable compound in both research and industrial applications. However, specific handling and safety measures should be observed due to the inherent properties of boronic acids.

5-METHYL-4-PROPOXY-1,3-PHENYLENEBISBORONIC ACID

850568-70-6: 5-Methyl-4-propoxy-1,3-phenylenebisboronic acid is a boronic acid derivative characterized by its unique structure, which includes two boronic acid functional groups attached to a phenylene backbone. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the methyl and propoxy substituents can influence its solubility, reactivity, and interaction with biological targets. Generally, boronic acids are known for their role in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, this compound may exhibit potential in drug development, particularly in targeting specific biomolecules due to its ability to interact with hydroxyl-containing compounds. Its stability, reactivity, and functionalization potential make it a valuable compound in both research and industrial applications. However, specific handling and safety measures should be observed due to the inherent properties of boronic acids.

5-Methyl-4-propoxy-1,3-phenylenediboronic acid

<p>5-Methyl-4-propoxybenzene-1,3-diboronic acid</p>

CAS 850568-70-6

5-METHYL-4-PROPOXY-1,3-PHENYLENEBISBORONIC ACID

5-Methyl-4-propoxy-1,3-phenylenediboronic acid

Ref: IN-DA004S9N

5-Methyl-4-propoxybenzene-1,3-diboronic acid

Ref: 54-OR1328