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| IUPAC Name: | 4,4,5,5-tetramethyl-2-(4-nitrophenyl)-1,3,2-dioxaborolane |
| Description: | Reactant involved in: Synthesis of aryl azides ; Arylation of allylic chlorides; Syntehsis of RNA conjugates; Alkoxycarbonylation; Synthesis of mTOR and PI3K inhibitors as antitumor agents; Electrooxidative synthesis of biaryls. |
| Molecular Weight: | 249.07 |
| Molecular Formula: | C12H16NO4B |
| Canonical SMILES: | B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)[N+](=O)[O-] |
| InChI: | InChI=1S/C12H16BNO4/c1-11(2)12(3,4)18-13(17-11)9-5-7-10(8-6-9)14(15)16/h5-8H,1-4H3 |
| InChI Key: | LUWACRUAJXZANC-UHFFFAOYSA-N |
| Boiling Point: | 357.5 °C at 760 mmHg |
| Melting Point: | 112-116 °C (lit.) |
| Flash Point: | Not applicable |
| Purity: | ≥ 95 % |
| Density: | 1.14 g/cm3 |
| MDL: | MFCD02179437 |
| LogP: | 2.41720 |
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Boronic Acids and Esters
2-(7,8-Difluoro-1-naphthyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4-(3,5-Dimethyl-1-pyrazolyl)phenylboronic Acid Pinacol Ester
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