(4-Methoxy-2-nitro-phenyl)boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a methoxy and a nitro substituent. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the methoxy group enhances its electron-donating properties, while the nitro group serves as an electron-withdrawing substituent, influencing the compound's reactivity and stability. (4-Methoxy-2-nitro-phenyl)boronic acid is often utilized in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, due to its ability to form stable complexes with transition metals. Additionally, it may have applications in medicinal chemistry and materials science, where boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in sensor technology and drug delivery systems.

(4-methoxy-2-nitro-phenyl)boronic acid

860034-09-9: (4-Methoxy-2-nitro-phenyl)boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a methoxy and a nitro substituent. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the methoxy group enhances its electron-donating properties, while the nitro group serves as an electron-withdrawing substituent, influencing the compound's reactivity and stability. (4-Methoxy-2-nitro-phenyl)boronic acid is often utilized in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, due to its ability to form stable complexes with transition metals. Additionally, it may have applications in medicinal chemistry and materials science, where boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in sensor technology and drug delivery systems.

CAS 860034-09-9

(4-methoxy-2-nitro-phenyl)boronic acid

4-Methoxy-2-nitrophenylboronic acid

Ref: IN-DA008FV9

4-Methoxy-2-nitrobenzeneboronic acid

Ref: 54-OR59360

(4-Methoxy-2-nitrophenyl)boronic acid

Ref: 10-F337948