Atomfair Pyren-1-ylboronic acid 1-Pyrenylboronic acid, 1-Pyreneboronic acid C16H11BO2

Description Pyren-1-ylboronic acid (CAS No. 164461-18-1) is a high-purity boronic acid derivative featuring a pyrene moiety, making it a valuable building block for organic synthesis and materials science applications. With the molecular formula C16H11BO2, this compound is widely utilized in Suzuki-Miyaura cross-coupling reactions due to its excellent reactivity with aryl halides. Its extended aromatic system enables applications in fluorescent probes, molecular sensors, and optoelectronic materials. Our product is rigorously tested for purity and stability, ensuring optimal performance in research and industrial settings. Available in various quantities, it is ideal for researchers seeking reliable and high-quality boronic acid reagents.

Description

Pyren-1-ylboronic acid (CAS No. 164461-18-1) is a high-purity boronic acid derivative featuring a pyrene moiety, making it a valuable building block for organic synthesis and materials science applications. With the molecular formula C₁₆H₁₁BO₂, this compound is widely utilized in Suzuki-Miyaura cross-coupling reactions due to its excellent reactivity with aryl halides. Its extended aromatic system enables applications in fluorescent probes, molecular sensors, and optoelectronic materials. Our product is rigorously tested for purity and stability, ensuring optimal performance in research and industrial settings. Available in various quantities, it is ideal for researchers seeking reliable and high-quality boronic acid reagents.

CAS No: 164461-18-1
Molecular Formula: C16H11BO2
Molecular Weight: 246.1
Exact Mass: 246.0852098
Monoisotopic Mass: 246.0852098
IUPAC Name: pyren-1-ylboronic acid
SMILES: B(C1=C2C=CC3=CC=CC4=C3C2=C(C=C1)C=C4)(O)O
Synonyms: Pyren-1-ylboronic Acid, 813-398-3, 1-Pyrenylboronic acid, 164461-18-1, 1-Pyreneboronic acid

Application

Pyren-1-ylboronic acid is commonly employed in the synthesis of conjugated polymers and organic semiconductors due to its ability to facilitate carbon-carbon bond formation. It serves as a key intermediate in the development of fluorescent dyes and sensors for detecting biologically relevant molecules. Researchers also utilize it in the fabrication of advanced materials for OLEDs and photovoltaic devices.

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