Description

2-(Naphthalen-1-yl)phenylboronic acid (CAS No. 500904-93-8) is a high-purity boronic acid derivative with the molecular formula C₁₆H₁₃BO₂. This compound is a valuable synthetic intermediate widely used in organic chemistry, particularly in Suzuki-Miyaura cross-coupling reactions, due to its robust reactivity and stability under various conditions. The IUPAC name for this compound is (2-naphthalen-1-ylphenyl)boronic acid, and it features a naphthalene moiety linked to a phenylboronic acid group, making it an excellent building block for constructing complex aromatic systems.

Our product is rigorously tested to ensure >98% purity (HPLC) and is supplied as a white to off-white crystalline powder. It is packaged under inert conditions to maintain stability and is ideal for pharmaceutical research, materials science, and catalysis applications. Store in a cool, dry place, protected from moisture and light to preserve its integrity.

Properties

• CAS Number: 500904-93-8
• Complexity: 294
• IUPAC Name: [2-(1-naphthyl)phenyl]boronic acid
• InChI: InChI=1S/C16H13BO2/c18-17(19)16-11-4-3-9-15(16)14-10-5-7-12-6-1-2-8-13(12)14/h1-11,18-19H
• InChI Key: AOYYQPPLTDMTIY-UHFFFAOYSA-N
• Exact Mass: 248.1008598
• Molecular Formula: C16H13BO2
• Molecular Weight: 248.1
• SMILES: B(C1=CC=CC=C1C2=CC=CC3=CC=CC=C32)(O)O
• Topological: 40.5
• Monoisotopic Mass: 248.1008598
• Synonyms: 500904-93-8, [2-(naphthalen-1-yl)phenyl]boronic acid, Boronic acid, [2-(1-naphthalenyl)phenyl]-, 2-(naphthalen-1-yl)phenylboronic acid, SCHEMBL590641

Application

2-(Naphthalen-1-yl)phenylboronic acid is primarily used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds for pharmaceuticals and advanced materials. It is also employed in the development of organic electronic materials, such as OLEDs and semiconductors, due to its conjugated aromatic structure. Researchers utilize this compound to create novel ligands for catalysis and as a precursor in medicinal chemistry for drug discovery.

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