Pinacol Vinylboronate CAS 75927-49-0 Purity >98.0% (GC) Factory High Purity
Manufacturer Supply With High Quality, Commercial Production
Chemical Name: Pinacol Vinylboronate CAS: 75927-49-0
| Chemical Name | Pinacol Vinylboronate |
| Synonyms | 2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; 4,4,5,5-Tetramethyl-2-vinyl-1,3,2-dioxaborolane; Vinylboronic Acid Pinacolester |
| CAS Number | 75927-49-0 |
| CAT Number | RF-PI1396 |
| Stock Status | In Stock, Production Scale Up to Tons |
| Molecular Formula | C8H15BO2 |
| Molecular Weight | 154.01 |
| Boiling Point | 52.0~54.0℃ |
| Density | 0.908 g/mL at 25℃ (lit.) |
| Brand | Ruifu Chemical |
| Item | Specifications |
| Appearance | Colorless to Light Yellow Liquid |
| Purity / Analysis Method | >98.0% (GC) |
| Moisture (K.F) | <0.50% |
| Total Impurities | <2.00% |
| Test Standard | Enterprise Standard |
| Usage | Pharmaceutical Intermediates |
Package: Bottle, 25kg/Barrel, or according to customer's requirement.
Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.
Pinacol Vinylboronate (CAS: 75927-49-0), Reagent used for: Suzuki-Miyaura coupling reactions; Mizoroki-Heck reactions (cascade reaction); Intramolecular Nozaki-Hiyama-Kishi reactions; Stereoselective Cu-catalyzed γ-selective and stereospecific coupling; Control of stereoselectivity and mechanistic portrait on intramolecular (4+1)-cycloaddition of dialkoxycarbenes; Regio- and stereoselective synthesis of trisubstituted alkenes via gold(I)-catalyzed hydrophosphoryloxylation of haloalkynes followed by Pd-catalyzed consecutive cross-coupling reactions; Asymmetric Birch reductive alkylation. Reagent used in Preparation of: Molecular tubes for lipid sensing; Enzymatic inhibitors, antibiotics, receptor analogs, and other biologically significant compounds.
