Description

3-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride) is a high-purity boronic acid derivative extensively utilized in organic synthesis, pharmaceutical research, and material science. With the molecular formula C₁₆H₁₃BO₂ and CAS number 881913-20-8, this compound serves as a crucial intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds under mild conditions. The product is supplied with varying amounts of anhydride, ensuring flexibility for diverse synthetic applications. Its naphthyl-phenyl backbone enhances stability and reactivity, making it ideal for constructing complex aromatic frameworks. Suitable for researchers and industrial scientists, this boronic acid is rigorously tested for quality and consistency, meeting the stringent demands of modern chemical research.

Properties

• CAS Number: 881913-20-8
• Complexity: 294
• IUPAC Name: [3-(1-naphthyl)phenyl]boronic acid
• InChI: InChI=1S/C16H13BO2/c18-17(19)14-8-3-7-13(11-14)16-10-4-6-12-5-1-2-9-15(12)16/h1-11,18-19H
• InChI Key: HFXYUCJLQZCNPD-UHFFFAOYSA-N
• Exact Mass: 248.1008598
• Molecular Formula: C16H13BO2
• Molecular Weight: 248.1
• SMILES: B(C1=CC(=CC=C1)C2=CC=CC3=CC=CC=C32)(O)O
• Topological: 40.5
• Monoisotopic Mass: 248.1008598
• Synonyms: 3-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride), 835-804-8, 881913-20-8, (3-(Naphthalen-1-yl)phenyl)boronic acid, 3-(1-naphthyl)phenylboronic acid, BORONIC ACID, [3-(1-NAPHTHALENYL)PHENYL]-, 3-(NAPHTHALEN-1-YL)PHENYLBORONIC ACID, (3-Naphthalen-1-ylphenyl)boronic acid, [3-(Naphthalen-1-yl)phenyl]boronic acid, 3-(1-Naphthyl)benzeneboronic acid, MFCD11045054, (3-(Naphthalen-1-yl)phenyl)boronic acid;3-(1-naphthalenyl)phenylboronic acid, [3-(1-Naphthyl)phenyl]boronic acid, BORONIC ACID,[3-(1-NAPHTHALENYL)PHENYL]-, SCHEMBL622947, DTXSID10730482, HFXYUCJLQZCNPD-UHFFFAOYSA-N, 3-(1-naphthyl) phenylboronic acid, AKOS016003520, CS-W001000, PB22452, (3-(Naphthalen-1-yl)phenyl)boronicacid, DS-15396, SY037995, N1131, 3-(naphthalen-1-yl)phenylboronic acid (contains varying amounts of Anhydride)

3-(1-Naphthyl)phenylboronic Acid is widely employed in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds, a key step in pharmaceutical and agrochemical development. It is also used in the preparation of advanced organic materials, including liquid crystals and OLED components. Researchers leverage its reactivity in constructing π-conjugated systems for optoelectronic applications. The compound’s stability and compatibility with various reaction conditions make it a versatile tool in medicinal chemistry for drug discovery.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

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

Hazard Classes and Categories

• Skin Irrit. 2 (100%)
• Eye Irrit. 2 (100%)

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