3-Chloro-4-methoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has both a chlorine and a methoxy substituent. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. The chlorine atom introduces a halogen functionality, which can enhance reactivity in cross-coupling reactions, while the methoxy group can influence the electronic properties of the aromatic ring, making it more nucleophilic. Boronic acids are known for their ability to form reversible complexes with diols, which is significant in various applications, including organic synthesis and medicinal chemistry. This compound is often utilized in Suzuki-Miyaura coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its unique structural features may contribute to its potential use in pharmaceuticals and agrochemicals, where selective reactivity and functionalization are essential. Safety data should be consulted for handling and storage, as with all chemical substances.

3-CHLORO-4-METHOXYPHENYLBORONIC ACID

175883-60-0: Akos Brn-0653, 3-Chloro-4-Methoxybenzeneboronic Acid, (3-Chloro-4-Ethoxyphenyl)Boronic Acid

(3-Chloro-4-methoxyphenyl)boronic acid

3-Chloro-4-methoxyphenylboronic Acid (contains varying amounts of Anhydride)

3-Chloro-4-methoxybenzeneboronic acid

Boronic acid, B-(3-chloro-4-methoxyphenyl)-

3-Chloro-4-methoxyphenylboronic acid

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CAS 175883-60-0: 3-CHLORO-4-METHOXYPHENYLBORONIC ACID

(3-Chloro-4-methoxyphenyl)boronic acid

Ref: 10-F219099

3-Chloro-4-methoxyphenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-C3056

3-Chloro-4-methoxybenzeneboronic acid

Ref: 54-OR13155

Boronic acid, B-(3-chloro-4-methoxyphenyl)-

Ref: IN-DA00219E

3-Chloro-4-methoxyphenylboronic acid

Ref: 7W-GK2041

3-Chloro-4-methoxyphenylboronic acid

Ref: 3D-FC59643