Atomfair 1-Naphthaleneboronic acid 1-Naphthylboronic acid C10H9BO2

Description 1-Naphthaleneboronic Acid (CAS 13922-41-3) is a high-purity boronic acid derivative with the molecular formula C10H9BO2, widely utilized in organic synthesis and pharmaceutical research. This compound, also known as naphthalen-1-ylboronic acid , features a boronic acid functional group attached to the 1-position of a naphthalene ring, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions. Its crystalline structure and stability under controlled conditions ensure reliable performance in catalytic applications. Ideal for researchers and scientists, our product is rigorously tested for purity (>98%) and consistency, meeting the stringent demands of advanced chemical synthesis. Available in various quantities, it is packaged…

Description

1-Naphthaleneboronic Acid (CAS 13922-41-3) is a high-purity boronic acid derivative with the molecular formula C₁₀H₉BO₂, widely utilized in organic synthesis and pharmaceutical research. This compound, also known as naphthalen-1-ylboronic acid, features a boronic acid functional group attached to the 1-position of a naphthalene ring, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions. Its crystalline structure and stability under controlled conditions ensure reliable performance in catalytic applications. Ideal for researchers and scientists, our product is rigorously tested for purity (>98%) and consistency, meeting the stringent demands of advanced chemical synthesis. Available in various quantities, it is packaged under inert conditions to maintain integrity and shelf life.

CAS No: 13922-41-3
Molecular Formula: C10H9BO2
Molecular Weight: 171.99
Exact Mass: 172.0695597
Monoisotopic Mass: 172.0695597
IUPAC Name: naphthalen-1-ylboronic acid
SMILES: B(C1=CC=CC2=CC=CC=C12)(O)O
Synonyms: 1-Naphthaleneboronic acid, 1-Naphthylboronic acid, 604-119-4, 13922-41-3, Naphthalene-1-boronic acid

Application

1-Naphthaleneboronic acid is extensively used in palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura couplings, to form biaryl compounds critical in drug discovery and material science. It serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic electronic materials. Researchers also employ it in the development of fluorescent probes and sensors due to its naphthalene backbone’s photophysical properties.

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