Identification | Back Directory | [Name]
4H-1-BENZOPYRAN-4-ONE | [CAS]
15485-80-0 | [Synonyms]
7-Hydroxy-4’-nitroisoflavone 7-Hydroxy-4'-nitroisoflavone 7-Hydroxy-4'-nitroisoflavone,98% 4H-1-Benzopyran-4-one, 7-hydroxy-3-(4-nitrophenyl)- | [Molecular Formula]
C15H9NO5 | [MDL Number]
MFCD01546432 | [MOL File]
15485-80-0.mol | [Molecular Weight]
283.24 |
Chemical Properties | Back Directory | [Melting point ]
290-292℃ | [Boiling point ]
530.8±50.0 °C(Predicted) | [density ]
1.494±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [form ]
Powder | [pka]
6.68±0.20(Predicted) | [color ]
Pale yellow | [Water Solubility ]
Slightly soluble in water. |
Hazard Information | Back Directory | [Uses]
7-Hydroxy-4'-nitroisoflavone is used in the synthesis of iso flavones, Synthesis of daidzin, soflavone amide derivatives. | [Synthesis]
In the first reaction flask, resorcinol (0.72 g, 6.5 mmol), p-nitrophenylacetic acid (1.0 g, 6.0 mmol), and BF3/Et2O (10 mL) were added and the reaction was stirred for 90 min at 75 °C. Upon completion of the reaction, the reaction mixture was cooled to below 10 °C and DMF (10 mL) was slowly added under stirring. In a second reaction flask, DMF (20 mL) was added, cooled to below 10 °C, PCl5 (2.0 g, 9 mmol) was added in batches and stirred at 55 °C for 30 min. After the reaction was completed, cooled to below 10 °C, the mixture in the first reaction flask was added slowly and the reaction was continued for 1 h at room temperature. Upon completion of the reaction, the reaction solution was poured into hot dilute hydrochloric acid (0.1 N) with stirring, the solid was precipitated, filtered, washed with water and dried. The crude product was recrystallized from methanol to give 0.36 g of product in 16.4% yield.MS (ESI): m/z = 284 [M + H]+. | [References]
[1] Patent: CN104672192, 2017, B. Location in patent: Paragraph 0050; 0051; 0052; 0053 |
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