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| IUPAC Name: | (2,4-dichlorophenyl)boronic acid |
| Description: | Reactant involved in: Suzuki coupling reactions with alkynyl bromides or aniline / thiophenol ; Selective hydroxylation to phenols. Reactant involved in synthesis of biologically active molecules including: N-hydroxyindole-2-carboxylates for use as lactate dehydrogenase inhibitors; Non-ATP competitive MK2 inhibitors. |
| Molecular Weight: | 190.82 |
| Molecular Formula: | C6H5Cl2O2B |
| Canonical SMILES: | B(C1=C(C=C(C=C1)Cl)Cl)(O)O |
| InChI: | InChI=1S/C6H5BCl2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,10-11H |
| InChI Key: | QNEGDGPAXKYZHZ-UHFFFAOYSA-N |
| Boiling Point: | 331.3 °C at 760 mmHg |
| Melting Point: | 246-249 °C (lit.) |
| Flash Point: | Not applicable |
| Purity: | ≥ 95 % |
| Density: | 1.47 g/cm3 |
| MDL: | MFCD00013930 |
| LogP: | 0.67320 |
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Boronic Acids and Esters
2-(7,8-Difluoro-1-naphthyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine
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