For research use only. Not for therapeutic Use.
2-Vinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(Cat No.:R044706)is a boronic ester featuring a vinyl group and a pinacol-derived dioxaborolane ring. This compound is commonly used in Suzuki–Miyaura cross-coupling reactions, enabling the formation of carbon–carbon bonds in the synthesis of complex organic molecules. Its vinyl functionality provides additional synthetic versatility for further functionalization or polymerization. The compound’s stability and solubility make it suitable for use in medicinal chemistry, material science, and agrochemical development. Its boron moiety also facilitates applications in the design of radiolabeled compounds and boron-containing pharmaceuticals.
CAS Number | 75927-49-0 |
Synonyms | 2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;?2-Vinyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; 4,4,5,5-Tetramethyl-2-(2-vinyl)-1,3,2-dioxaborolane; 4,4,5,5-Tetramethyl-2-vinyl-1,3,2-dioxaborolane; Vinylboronic Acid Pinacol Ester |
Molecular Formula | C8H15BO2 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
InChI | InChI=1S/C8H15BO2/c1-6-9-10-7(2,3)8(4,5)11-9/h6H,1H2,2-5H3 |
InChIKey | DPGSPRJLAZGUBQ-UHFFFAOYSA-N |
SMILES | B1(OC(C(O1)(C)C)(C)C)C=C |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |