B-1-Naphthalenyl-boronic Acid

• CAT Number: R023826
• CAS Number: 13922-41-3
• Molecular Formula: C10H9BO2
• Molecular Weight: 171.99
• Purity: ≥95%
• Synonyms: 1-Naphthaleneboronic Acid; 1-Naphthalenyl-boronic Acid; (1-Naphthalenyl)boronic Acid; (Naphthalen-1-yl)boronic Acid; 1-Naphthylboric Acid; 1-Naphthylboronic Acid; NSC 78936; α-Naphthaleneboronic Acid; α-Naphthylboronic Acid
• Storage: Store at RT
• IUPAC Name: naphthalen-1-ylboronic acid
• InChI: InChI=1S/C10H9BO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7,12-13H
• InChIKey: HUMMCEUVDBVXTQ-UHFFFAOYSA-N
• SMILES: B(C1=CC=CC2=CC=CC=C12)(O)O

B-1-Naphthalenylboronic acid(CAT: R023826) is an arylboronic acid derivative featuring a boronic acid group attached to the 1-position of the naphthalene ring. This compound is widely used as a building block in Suzuki–Miyaura cross-coupling reactions, enabling the formation of C–C bonds for the synthesis of biaryl and polycyclic aromatic structures. The extended π-conjugation of the naphthalene moiety makes it particularly valuable in organic electronics, materials science, and pharmaceutical development. Its reactivity and structural rigidity allow for the creation of functionally diverse aromatic frameworks, making it an essential intermediate in the construction of ligands, dyes, and bioactive molecules.