IUPAC Name: | [(E)-prop-1-enyl]boronic acid |
Description: | Reactant for: Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions; Cu(II)-mediated Ullmann-type coupling. Reactant for preparation of: Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases; Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling; Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization; Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones Reactant for; Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions ; Cu(II)-mediated Ullmann-type coupling ; Palladium-catalyzed Sonogashira cross-coupling Reactant for preparation of; Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases ; Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling ; Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization ; Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones. |
Molecular Weight: | 85.90 |
Molecular Formula: | C3H7O2B |
Canonical SMILES: | B(C=CC)(O)O |
InChI: | InChI=1S/C3H7BO2/c1-2-3-4(5)6/h2-3,5-6H,1H3/b3-2+ |
InChI Key: | CBMCZKMIOZYAHS-NSCUHMNNSA-N |
Boiling Point: | 175.6 °C at 760 mmHg |
Melting Point: | 123-127 °C (lit.) |
Flash Point: | Not applicable |
Purity: | ≥ 95.0 % |
Density: | 0.969 g/cm3 |
Appearance: | Solid |
Storage: | 2-8 °C |
LogP: | -0.42550 |
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Boronic Acids and Esters
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