[2-Methyl-4-(1-methylethoxy)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, making it useful in various applications, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a methyl group and an ethoxy group, contributing to its hydrophobic characteristics. The boronic acid moiety imparts unique reactivity, allowing it to participate in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the ethoxy group enhances its solubility in organic solvents, facilitating its use in diverse chemical environments. The compound's structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators that target specific biological pathways. Overall, [2-methyl-4-(1-methylethoxy)phenyl]boronic acid exemplifies the versatility of boronic acids in synthetic organic chemistry and their significance in pharmaceutical research.

[2-methyl-4-(1-methylethoxy)phenyl]boronic acid

871126-21-5: [2-Methyl-4-(1-methylethoxy)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, making it useful in various applications, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a methyl group and an ethoxy group, contributing to its hydrophobic characteristics. The boronic acid moiety imparts unique reactivity, allowing it to participate in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of the ethoxy group enhances its solubility in organic solvents, facilitating its use in diverse chemical environments. The compound's structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators that target specific biological pathways. Overall, [2-methyl-4-(1-methylethoxy)phenyl]boronic acid exemplifies the versatility of boronic acids in synthetic organic chemistry and their significance in pharmaceutical research.

CAS 871126-21-5

[2-methyl-4-(1-methylethoxy)phenyl]boronic acid

4-Isopropoxy-2-methylphenylboronic acid

Ref: IN-DA004LAW

4-Isopropoxy-2-methylbenzeneboronic acid 98%

Ref: 54-OR4237

(4-Isopropoxy-2-methylphenyl)boronic acid

Ref: 10-F219673