Atomfair 2-Chlorophenylboronic acid C6H6BClO2 CAS 3900-89-8

Description

2-Chlorophenylboronic acid (CAS No. 3900-89-8) is a high-purity boronic acid derivative with the molecular formula C₆H₆BClO₂. This organoboron compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and stability. The product is supplied as a white to off-white crystalline powder with a purity of ≥95.0%, ensuring consistent performance in research and industrial applications. It is soluble in common organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO), making it versatile for various reaction conditions. Suitable for pharmaceutical, agrochemical, and material science research, this reagent is rigorously tested for quality and stored under optimal conditions to maintain its integrity.

Properties

• CAS Number: 3900-89-8
• Complexity: 110
• IUPAC Name: (2-chlorophenyl)boronic acid
• InChI: InChI=1S/C6H6BClO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H
• InChI Key: RRCMGJCFMJBHQC-UHFFFAOYSA-N
• Exact Mass: 156.0149373
• Molecular Formula: C6H6BClO2
• Molecular Weight: 156.38
• SMILES: B(C1=CC=CC=C1Cl)(O)O
• Topological: 40.5
• Monoisotopic Mass: 156.0149373
• Synonyms: 2-Chlorophenylboronic acid, 3900-89-8, (2-chlorophenyl)boronic acid, 2-chlorobenzeneboronic acid, o-chlorophenylboronic acid, MFCD00674012, 2-chlorophenyl boronic acid, 2-Chlorophenylboronicacid, Boronic acid, (2-chlorophenyl)-, (o-Chlorophenyl)boronic Acid; 2-Chlorobenzeneboronic Acid; 2-Chlorophenylboronic Acid; (2-Chlorophenyl)-boronic Acid; o-Chloro-benzeneboronic Acid, o-chlorphenylboronic acid, o-chlorophenyl boronic acid, (2-chlorophenyl)boronicacid, 2-chloro phenylboronic acid, 2-chloro-phenylboronic acid, 2-chlorophenyl-boronic acid, SCHEMBL4129, 2-chlorobenzene boronic acid, 2-chloro phenyl boronic acid, 2-chloro-phenyl boronic acid, 2-chloro-phenyl-boronic acid, 2-chloro benzene boronic acid, 2-chloro-benzene boronic acid, 2-chloro-benzene-boronic acid, AKOS BRN-0009, (2-chlorophenyl) boronic acid, (2-chlorophenyl)-boronic acid, SCHEMBL29183868, DTXSID80370213, ALBB-006098, BCP22739, CS-D1476, O-CHLORO-BENZENEBORONIC ACID, SBB048063, STK503705, AKOS000266633, AB06914, AC-5347, AS-2594, BCP9000256, 2-Chlorophenylboronic acid, >=95.0%, NCGC00249464-01, FC117160, SY007772, DB-012341, C1705, EN300-114510, Z381540900, 2-Chlorophenylboronic acid (contains varying amounts of Anhydride)

2-Chlorophenylboronic acid is primarily used as a key intermediate in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds, which are essential in drug discovery and materials science. It serves as a building block in the synthesis of pharmaceuticals, agrochemicals, and advanced functional materials. Researchers also employ it in the development of boron-based sensors and catalysts due to its unique reactivity.

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