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2-(Tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-ol
For research use only. Not for therapeutic Use.
2-(Tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-ol(Cat No.:L007350), is a significant organic compound widely used in chemical synthesis. Its molecular structure comprises a boron-containing boronate ester moiety and an allylic alcohol group. This compound is highly valued in the field of organic chemistry as a versatile reagent for various transformations, including Suzuki-Miyaura cross-coupling reactions. The boronate functionality enables the compound to participate in diverse C-C bond-forming reactions, making it a valuable tool for the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials.
Catalog Number | L007350 |
CAS Number | 1294009-05-4 |
Molecular Formula | C9H17BO3 |
Purity | ≥95% |
IUPAC Name | 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-ol |
InChI | InChI=1S/C9H17BO3/c1-7(6-11)10-12-8(2,3)9(4,5)13-10/h11H,1,6H2,2-5H3 |
InChIKey | SDQIEQJUQUFRHB-UHFFFAOYSA-N |
SMILES | B1(OC(C(O1)(C)C)(C)C)C(=C)CO |