[2-(Benzyloxy)-5-chlorophenyl]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 chemical reactions, particularly in Suzuki coupling reactions. This compound features a chlorophenyl group, which contributes to its electronic properties and reactivity. The benzyloxy substituent enhances its solubility and stability in organic solvents. Typically, boronic acids exhibit moderate acidity due to the presence of the boron atom, which can coordinate with Lewis bases. This compound is often utilized in medicinal chemistry and materials science for the synthesis of complex organic molecules. Its structural features suggest potential applications in drug development and as a building block in organic synthesis. Additionally, the presence of the chlorine atom can influence the compound's reactivity and interaction with biological targets. Overall, [2-(benzyloxy)-5-chlorophenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry.

[2-(benzyloxy)-5-chlorophenyl]boronic acid

612832-83-4: boronic acid, B-[5-chloro-2-(phenylmethoxy)phenyl]-, (2-(Benzyloxy)-5-chlorophenyl)boronicacid, 2-Benzyloxy-5-Chlorobenzeneboronic Acid, 2-Benzyloxy-5-Chlorophenylboronic Acid

(2-(Benzyloxy)-5-chlorophenyl)boronic acid

2-Benzyloxy-5-chlorobenzeneboronic acid

2-Benzyloxy-5-chlorophenylboronic Acid (contains varying amounts of Anhydride)

2-BENZYLOXY-5-CHLOROPHENYLBORONIC ACID

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CAS 612832-83-4: [2-(benzyloxy)-5-chlorophenyl]boronic acid

(2-(Benzyloxy)-5-chlorophenyl)boronic acid

Ref: 10-F212340

2-Benzyloxy-5-chlorobenzeneboronic acid

Ref: 54-OR7153

2-Benzyloxy-5-chlorophenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-B5076

2-BENZYLOXY-5-CHLOROPHENYLBORONIC ACID

Ref: IN-DA00EB4B

2-Benzyloxy-5-chlorophenylboronicacid

Ref: 3D-FB147553