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| IUPAC Name: | 1-phenylethenylboronic acid |
| Description: | Reactant involved in: Halogenation of alkynes for preparation of enol esters; Liebeskind-Srogl cross-coupling; Homocoupling of arylboronic acids for synthesis of biaryls; Iterative cross-coupling of boronate building blocks; Enantioselective hydrogenation of hydroxyphenyl styrenes; Samarium diiodide-mediated cyclization for synthesis of substituted benzannulated cyclooctanol derivatives; Suzuki-Miyaura cross-coupling for synthesis of C-6-substituted uridine phosphonates. |
| Molecular Weight: | 147.97 |
| Molecular Formula: | C8H9O2B |
| Canonical SMILES: | B(C(=C)C1=CC=CC=C1)(O)O |
| InChI: | InChI=1S/C8H9BO2/c1-7(9(10)11)8-5-3-2-4-6-8/h2-6,10-11H,1H2 |
| InChI Key: | YJCPVMYUISTDKG-UHFFFAOYSA-N |
| Boiling Point: | 321.1 °C at 760 mmHg |
| Melting Point: | 125 °C (dec.) (lit.) |
| Flash Point: | Not applicable |
| Purity: | 95 % |
| Density: | 1.09 g/cm3 |
| Storage: | 2-8 °C |
| MDL: | MFCD01074578 |
| LogP: | 0.71180 |
Catalog: BB042560
(2-(Trifluoromethyl)pyrimidin-5-yl)boronic acid
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Catalog: BB054456
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Catalog: BB079598
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Flexible batch size for diverse industrial demandsRelated Functional Groups
Boronic Acids and Esters
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