5-Borono-4-chloro-2-methoxy-benzoic acid is an organic compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. The presence of a chlorine atom and a methoxy group on the aromatic ring contributes to its reactivity and solubility properties. This compound typically appears as a solid at room temperature and is soluble in polar organic solvents. Its structure allows for potential applications in drug development, particularly in the synthesis of biologically active molecules. The boronic acid moiety can participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is a valuable reaction in organic synthesis. Additionally, the compound may exhibit specific biological activities, making it of interest in pharmaceutical research. Proper handling and storage are essential due to the potential reactivity of the boronic acid group, and safety precautions should be observed when working with this substance.

5-borono-4-chloro-2-methoxy-benzoic acid

957066-09-0: 5-Borono-4-chloro-2-methoxy-benzoic acid is an organic compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. The presence of a chlorine atom and a methoxy group on the aromatic ring contributes to its reactivity and solubility properties. This compound typically appears as a solid at room temperature and is soluble in polar organic solvents. Its structure allows for potential applications in drug development, particularly in the synthesis of biologically active molecules. The boronic acid moiety can participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is a valuable reaction in organic synthesis. Additionally, the compound may exhibit specific biological activities, making it of interest in pharmaceutical research. Proper handling and storage are essential due to the potential reactivity of the boronic acid group, and safety precautions should be observed when working with this substance.

CAS 957066-09-0

5-borono-4-chloro-2-methoxy-benzoic acid

5-Carboxy-2-chloro-4-methoxyphenylboronic acid

Ref: IN-DA006BLB

5-Carboxy-2-chloro-4-methoxybenzeneboronic acid

Ref: 54-OR59414