Substance
ID:333888
Names and Identifiers
IUPAC name
4,4,5,5-tetramethyl-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane
IUPAC Traditional name
bis(pinacolato)diboron
Synonyms
4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bi-1,3,2-dioxaborolaneBis(pinacolato)diboron双戊酰二硼双联频哪醇硼酸酯
Properties
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
MSDS Link
German water hazard class
3
Physical Property
Melting Point
137-140 °C(lit.)
Product Information
Purity
99%
Empirical Formula (Hill Notation)
C12H24B2O4
Molecule Details
Application
Reagent used for the cis-vicinal diborylation of acetylenes and olefins with Pt catalysis; borylation of aromatics by Pd catalysis.1
Substrate used in a new palladium-catalyzed cyclization of 1,6-enynes leading to homoallylic alkylboronates.
Used to construct a tetramethylpyrrolidine nitroxide scaffold for the synthesis of paramagnetic heterocycles by Suzuki coupling.
Packaging
1, 5, 25 g in glass bottle
100 g in poly bottle
500 g in glass bottle
Reagent used for the cis-vicinal diborylation of acetylenes and olefins with Pt catalysis; borylation of aromatics by Pd catalysis.1
Substrate used in a new palladium-catalyzed cyclization of 1,6-enynes leading to homoallylic alkylboronates.
Used to construct a tetramethylpyrrolidine nitroxide scaffold for the synthesis of paramagnetic heterocycles by Suzuki coupling.
Packaging
1, 5, 25 g in glass bottle
100 g in poly bottle
500 g in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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