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Sku SC05-1030_5_G
US-Strem
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Product Information

Product Name
1-Naphthylboronic acid, min. 97%
Brand Name
US-Strem
Product Number
05-1030
CAS
13922-41-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
254532
IUPAC Name
naphthalen-1-ylboronic acid
InChI Key
HUMMCEUVDBVXTQ-UHFFFAOYSA-N
SMILES
B(C1=CC=CC2=CC=CC=C12)(O)O

Description

Technical Notes:
1. Reagent used for the palladium-catalyzed aryl borylation of aryl halides.
2.Reagent used for the copper-catalyzed ß-boration of a,ß-unsaturated carbonyl compounds. 3. Reagent used for the nickel-catayzed (het)aryl borylation of aryl halides.
4. Reagent used for the palladium-catalyzed borylation of allylic alcohols
References:
1. J. Am. Chem. Soc. 2012, 134, 11667. 2. Org. L ett.2011, 13, 4684.
3.J. Org. Chem. 2013, 78, 6427.
4.Angew. Chem., Int. Ed. 2012, 51, 13050.

References Data Source From Pubchem

Polymer Supported Ruthenium and Palladium Based Bi-Metallic Catalyst for Tandem Cross-Coupling/Transfer Hydrogenation

Publication Name: Catalysis Letters
Publication Date: 2026-02-17
DOI: 10.1007/s10562-025-05297-x

New applications of kinetic data. The development of machine learning kinetic models for the Suzuki—Miyaura reaction

Publication Name: Russian Chemical Bulletin
Publication Date: 2025-11
DOI: 10.1007/s11172-025-4812-2

Synthesis of new aryl derivatives of isobornylphenols by the Suzuki reaction

Publication Name: Russian Chemical Bulletin
Publication Date: 2024-12
DOI: 10.1007/s11172-024-4469-2

Recent synthetic strategies for N-arylation of pyrrolidines: a potential template for biologically active molecules

Publication Name: Molecular Diversity
Publication Date: 2024-07-24
DOI: 10.1007/s11030-024-10924-7