Atomfair Dibutyl Vinylboronate (stabilized with Phenothiazine) C10H21BO2

Description Dibutyl Vinylboronate (stabilized with Phenothiazine) is a highly specialized organoboron compound with the molecular formula C10H21BO2and CAS number 6336-45-4 . This reagent is stabilized with phenothiazine to enhance its shelf life and handling safety. It is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile vinylboron precursor. The compound is characterized by its clear to pale yellow liquid appearance and must be stored under inert conditions to prevent degradation. Ideal for researchers and chemists, this high-purity reagent is packaged under nitrogen to ensure optimal stability and performance in sensitive applications.

Description

Dibutyl Vinylboronate (stabilized with Phenothiazine) is a highly specialized organoboron compound with the molecular formula C₁₀H₂₁BO₂ and CAS number 6336-45-4. This reagent is stabilized with phenothiazine to enhance its shelf life and handling safety. It is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile vinylboron precursor. The compound is characterized by its clear to pale yellow liquid appearance and must be stored under inert conditions to prevent degradation. Ideal for researchers and chemists, this high-purity reagent is packaged under nitrogen to ensure optimal stability and performance in sensitive applications.

CAS No: 6336-45-4
Molecular Formula: C10H21BO2
Molecular Weight: 184.09
Exact Mass: 184.1634601
Monoisotopic Mass: 184.1634601
IUPAC Name: dibutoxy(ethenyl)borane
SMILES: B(C=C)(OCCCC)OCCCC
Synonyms: Dibutyl Vinylboronate (stabilized with Phenothiazine), 663-504-5, Vinylboronic acid dibutyl ester, 6336-45-4, dibutyl vinylboronate

Application

Dibutyl Vinylboronate is a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic syntheses. It is particularly valuable in pharmaceutical research for constructing vinyl-substituted aromatic systems. Additionally, it finds use in material science for developing advanced polymers and functionalized materials. Its stabilization with phenothiazine ensures reliable performance in air-sensitive reactions.

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