Description

(10-Phenylanthracen-9-yl)boronic acid (CAS No. 334658-75-2) is a high-purity boronic acid derivative with the molecular formula C₂₀H₁₅BO₂. This compound features a phenyl-substituted anthracene core functionalized with a boronic acid group, making it a valuable building block in organic synthesis and materials science. With its rigid aromatic structure, it is particularly useful in Suzuki-Miyaura cross-coupling reactions for constructing complex polycyclic aromatic systems. Ideal for researchers in pharmaceuticals, OLED materials, and polymer chemistry, this product is rigorously tested for consistency and purity. Available in gram to kilogram quantities, it is supplied with comprehensive analytical data (NMR, HPLC, MS) to ensure reproducibility in your experiments.

Properties

• CAS Number: 334658-75-2
• Complexity: 369
• IUPAC Name: (10-phenyl-9-anthryl)boronic acid
• InChI: InChI=1S/C20H15BO2/c22-21(23)20-17-12-6-4-10-15(17)19(14-8-2-1-3-9-14)16-11-5-7-13-18(16)20/h1-13,22-23H
• InChI Key: RVPCPPWNSMAZKR-UHFFFAOYSA-N
• Exact Mass: 298.1165099
• Molecular Formula: C20H15BO2
• Molecular Weight: 298.1
• SMILES: B(C1=C2C=CC=CC2=C(C3=CC=CC=C13)C4=CC=CC=C4)(O)O
• Topological: 40.5
• Monoisotopic Mass: 298.1165099
• Synonyms: (10-phenylanthracen-9-yl)boronic acid, 334658-75-2, DTXSID90623823, DTXCID80574577, 805-893-8, 10-Phenyl-9-anthraceneboronic Acid, 10-Phenyl-9-anthracene boronic acid, 10-Phenylantrhacen-9-yl boronic acid, 10-Phenylanthracene-9-boronic acid, MFCD11111989, Boronic acid, (10-phenyl-9-anthracenyl)-, (10-phenylanthracen-9-yl)boronicacid, SCHEMBL338760, BCP05172, (10-Phenyl-9-anthryl)boronic acid, BBL103134, STL556944, 10-Phenyl-9-anthraceneboronic acid (contains varying amounts of Anhydride), AKOS015901173, CS-W000914, SB66521, AC-24437, AS-19009, SY022637, SY299610, DB-002309, P1984, 10-(Phenyl-2,3,4,5,6-d5)anthracene-9-boronic Acid, 10-Phenyl-9-anthraceneboronic Acid(contains varying amounts of Anhydride)

Application

(10-Phenylanthracen-9-yl)boronic acid is widely employed in Suzuki-Miyaura cross-coupling reactions to synthesize extended π-conjugated systems for organic electronic applications. It serves as a key intermediate in the development of anthracene-based fluorescent probes and optoelectronic materials. Researchers also utilize it to construct molecular scaffolds for drug discovery and supramolecular chemistry studies.

Safety and Hazards

GHS Hazard Statements

• H301 (33.3%): Toxic if swallowed [Danger Acute toxicity, oral]
• H315 (66.7%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (66.7%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

• P264, P264+P265, P270, P280, P301+P316, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, P405, and P501

Hazard Classes and Categories

• Acute Tox. 3 (33.3%)
• Skin Irrit. 2 (66.7%)
• Eye Irrit. 2 (66.7%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.