Pinacol Vinylboronate CAS 75927-49-0 Purity >98.0% (GC) Factory High Purity

Chemical Name: Pinacol Vinylboronate  CAS: 75927-49-0 Purity: >98.0% (GC) Appearance: Colorless to Light Yellow Liquid High Quality, Commercial Production E-Mail: alvin@ruifuchem.com

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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.Manufacturer Supply With High Quality, Commercial Production  Chemical Name: Pinacol Vinylboronate CAS: 75927-49-0
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

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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

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Application:

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.

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