Description

4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride) is a high-purity boronic acid derivative with the molecular formula C₁₆H₁₃BO₂ and CAS number 870774-25-7. This compound, also known by its IUPAC name (4-naphthalen-1-ylphenyl)boronic acid, is a valuable building block in organic synthesis and pharmaceutical research. The product may contain varying amounts of anhydride, as indicated. It is characterized by its naphthyl-phenyl backbone, which enhances its utility in cross-coupling reactions such as Suzuki-Miyaura couplings. Suitable for researchers and scientists, this reagent is provided with detailed analytical documentation to ensure reproducibility and performance in demanding applications. Store in a cool, dry place under inert conditions to maintain stability.

Properties

• CAS Number: 870774-25-7
• Complexity: 286
• IUPAC Name: [4-(1-naphthyl)phenyl]boronic acid
• InChI: InChI=1S/C16H13BO2/c18-17(19)14-10-8-13(9-11-14)16-7-3-5-12-4-1-2-6-15(12)16/h1-11,18-19H
• InChI Key: BQHVXFQXTOIMQM-UHFFFAOYSA-N
• Exact Mass: 248.1008598
• Molecular Formula: C16H13BO2
• Molecular Weight: 248.1
• SMILES: B(C1=CC=C(C=C1)C2=CC=CC3=CC=CC=C32)(O)O
• Topological: 40.5
• Monoisotopic Mass: 248.1008598
• Synonyms: 4-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride), 678-309-0, 870774-25-7, 4-(naphthalen-1-yl)phenylboronic acid, 4-(1-Naphthyl)benzeneboronic Acid, 4-(1-Naphthyl)phenylboronic Acid, (4-(naphthalen-1-yl)phenyl)boronic acid, MFCD08669639, (4-naphthalen-1-ylphenyl)boronic acid, [4-(Naphthalen-1-yl)phenyl]boronic acid, 4-(1-naphthalenyl)phenylboronic acid, Boronic acid, [4-(1-naphthalenyl)phenyl]-, 4-(1-Naphthyl) phenylboronic Acid, 4-(NAPHTH-1-YL)BENZENEBORONIC ACID, SCHEMBL431998, DTXSID30657203, 4-(1-Naphthyl)phenyl boronic acid, SBB052595, 4-(Naphthalene-1-yl)phenylboronicacid, AKOS015855882, CS-W000991, DS-1129, SB66987, 4-(Naphthalen-1-yl)phenyl boronic acid, 4-(naphthalene-1-yl)phenyl boronic acid, AC-24821, SY030416, DB-012323, N0798, 4-Phenyl(napthalene-1-yl)boronic acid, AldrichCPR, 4-(1-Naphthyl)benzeneboronic acid(contains varying amounts of Anhydride)

Application

4-(1-Naphthyl)phenylboronic Acid is widely used as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and materials science research. It serves as a versatile coupling partner in Suzuki-Miyaura reactions for constructing biaryl systems. The compound is also employed in the development of sensors and ligands due to its boronic acid functionality. Researchers utilize it in the preparation of advanced materials, including OLEDs and liquid crystals.

Safety and Hazards

GHS Hazard Statements

• H315 (66.7%): Causes skin irritation [Warning Skin corrosion/irritation]
• H318 (33.3%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
• H319 (66.7%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

• P264, P264+P265, P280, P302+P352, P305+P351+P338, P305+P354+P338, P317, P321, P332+P317, P337+P317, and P362+P364

Hazard Classes and Categories

• Skin Irrit. 2 (66.7%)
• Eye Dam. 1 (33.3%)
• 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.