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| IUPAC Name: | (2-nitrophenyl)boronic acid |
| Description: | Boronic acid catalyst used for: Mild and selective dipolar cycloadditions of unsaturated carboxylic acids with azides; Transposition of allylic alcohols and Meyer-Schuster rearrangements. Reactant involved in: Suzuki-Miyaura cross-coupling reactions with aryl halides or nitroarenediazonium tetrafluoroborates; Copper-catalyzed halogenation; Oxidative arylation of aminopyrazolyl disulfides. Used in a preparation of unsymmetrical 2,2'-dinitrobiphenyls via Suzuki-Miyaura cross-coupling with nitrophenyl halides. |
| Molecular Weight: | 166.93 |
| Molecular Formula: | C6H6NO4B |
| Canonical SMILES: | B(C1=CC=CC=C1[N+](=O)[O-])(O)O |
| InChI: | InChI=1S/C6H6BNO4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4,9-10H |
| InChI Key: | SFUIGUOONHIVLG-UHFFFAOYSA-N |
| Boiling Point: | 374.8 °C at 760 mmHg |
| Melting Point: | 155-160 °C |
| Flash Point: | Not applicable |
| Purity: | 99 % |
| Density: | 1.40 ± 0.1 g/mL (predicted) |
| Appearance: | White powder |
| MDL: | MFCD00161358 |
| LogP: | -0.20220 |
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Boronic Acids and Esters
2-(3-Hydroxyphenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
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