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| IUPAC Name: | (3-nitrophenyl)boronic acid |
| Description: | Reactant involved in: Copper-catalyzed arylation; Palladium-catalyzed decarboxylative coupling; Suzuki-Miyaura cross-coupling; Oxidative carbocyclization / arylation; Addition to arylpropargyl alcohols. Additionally used as a reactant for synthesizing biologically active molecules such as: Inhibitors of angiogenesis; Biaryl-olefins with antiproliferative activities Catalyzes ene carbocyclization of acetylenic dicarbonyl compounds. |
| 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)5-2-1-3-6(4-5)8(11)12/h1-4,9-10H |
| InChI Key: | ZNRGSYUVFVNSAW-UHFFFAOYSA-N |
| Boiling Point: | 363.3 ℃ at 760 mmHg |
| Melting Point: | 284-285 ℃ (dec.) (lit.) |
| Purity: | ≥ 97 % |
| Density: | 1.4 g/cm3 |
| Appearance: | Powder |
| Storage: | Keep in dark place, Sealed in dry, Room Temperature |
| MDL: | MFCD00007193 |
| LogP: | -0.20220 |
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