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| IUPAC Name: | naphthalen-2-ylboronic acid |
| Description: | Used in a study of an enantioselective rhodium-catalyzed addition of aryl boronic acids to 2,2,2-trifluoroacetophenones leading to chiral, tertiary trifluoromethyl alcohols. Also employed in a study of a palladium-catalyzed addition of aryl boronic acids to nitriles providing aryl ketones and to aryloxy nitriles providing benzofurans. |
| Molecular Weight: | 171.99 |
| Molecular Formula: | C10H9O2B |
| Canonical SMILES: | B(C1=CC2=CC=CC=C2C=C1)(O)O |
| InChI: | InChI=1S/C10H9BO2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,12-13H |
| InChI Key: | KPTRDYONBVUWPD-UHFFFAOYSA-N |
| Boiling Point: | 381.9 °C at 760 mmHg |
| Melting Point: | 269-275 °C |
| Flash Point: | Not applicable |
| Purity: | 99 % |
| Density: | 1.21 ± 0.1 g/mL (predicted) |
| Appearance: | White powder |
| MDL: | MFCD00236051 |
| LogP: | 0.51960 |
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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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