2-Chloro-5-(dihydroxyboranyl)benzoic acid is an organic compound characterized by its aromatic structure, which includes a benzoic acid moiety substituted with a chlorine atom and a dihydroxyboranyl group. The presence of the chlorine atom at the 2-position and the dihydroxyboranyl group at the 5-position contributes to its unique reactivity and potential applications in various chemical reactions, particularly in organic synthesis and medicinal chemistry. The dihydroxyboranyl group can act as a Lewis acid, facilitating interactions with nucleophiles. This compound is likely to exhibit moderate solubility in polar solvents due to the presence of the carboxylic acid and hydroxyl groups, while its aromatic nature may impart some hydrophobic characteristics. Additionally, the compound may participate in hydrogen bonding due to the hydroxyl groups, influencing its physical properties and reactivity. Overall, 2-chloro-5-(dihydroxyboranyl)benzoic acid represents a versatile building block in the synthesis of more complex organic molecules.

2-chloro-5-(dihydroxyboranyl)benzoic acid

913835-32-2: 2-Chloro-5-(dihydroxyboryl)benzoic acid, 5-Borono-2-chlorobenzoicacid, Benzoic Acid, 5-Borono-2-Chloro-, 3-Carboxy-4-Chlorobenzeneboronic Acid

3-Carboxy-4-chlorobenzeneboronic acid

3-CARBOXY-4-CHLOROBENZENEBORONIC ACID

5-Borono-2-chlorobenzoic acid

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CAS 913835-32-2: 2-chloro-5-(dihydroxyboranyl)benzoic acid

3-Carboxy-4-chlorobenzeneboronic acid

Ref: 54-OR9342

3-CARBOXY-4-CHLOROBENZENEBORONIC ACID

Ref: IN-DA00GTDG

5-Borono-2-chlorobenzoic acid

Ref: 10-F078092

5-Borono-2-chlorobenzoic acid

Ref: 3D-FB140433

3-Carboxy-4-chlorophenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-C3209