Atomfair Boric acid, pinacol ester C6H13BO3

Description Boric Acid Pinacol Ester (CAS No. 25240-59-9) is a high-purity organoboron compound with the molecular formula C6H13BO3. Also known as 2-hydroxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane , this versatile reagent is widely utilized in organic synthesis, catalysis, and as a boron source in cross-coupling reactions. Its stable cyclic ester structure makes it an excellent precursor for Suzuki-Miyaura couplings, hydroboration, and other transition-metal-catalyzed transformations. This product is rigorously tested for purity and consistency, ensuring optimal performance in research and industrial applications. Suitable for use under inert conditions, it is supplied in moisture-resistant packaging to maintain integrity.

Description

Boric Acid Pinacol Ester (CAS No. 25240-59-9) is a high-purity organoboron compound with the molecular formula C₆H₁₃BO₃. Also known as 2-hydroxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, this versatile reagent is widely utilized in organic synthesis, catalysis, and as a boron source in cross-coupling reactions. Its stable cyclic ester structure makes it an excellent precursor for Suzuki-Miyaura couplings, hydroboration, and other transition-metal-catalyzed transformations. This product is rigorously tested for purity and consistency, ensuring optimal performance in research and industrial applications. Suitable for use under inert conditions, it is supplied in moisture-resistant packaging to maintain integrity.

CAS No: 25240-59-9
Molecular Formula: C6H13BO3
Molecular Weight: 143.98
Exact Mass: 144.0957744
Monoisotopic Mass: 144.0957744
IUPAC Name: 2-hydroxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
SMILES: B1(OC(C(O1)(C)C)(C)C)O
Synonyms: Boric acid, pinacol ester, 800-445-8, 25240-59-9, 2-hydroxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, Boric acid pinacol ester

Application

Boric Acid Pinacol Ester is commonly employed as a boronating agent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds. It serves as a key intermediate in pharmaceutical and agrochemical research due to its stability and reactivity. Additionally, it is used in polymer chemistry and materials science for modifying organic frameworks with boron-containing functional groups.

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