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| | 2-Nitro-4-fluorophenol Basic information |
| | 2-Nitro-4-fluorophenol Chemical Properties |
| Melting point | 75-77 °C (lit.) | | Boiling point | 234.1±20.0 °C(Predicted) | | density | 1.4306 (estimate) | | storage temp. | Inert atmosphere,Room Temperature | | pka | 6.76±0.14(Predicted) | | form | powder to crystal | | color | Orange to Green to Amber | | BRN | 1950412 | | InChI | InChI=1S/C6H4FNO3/c7-4-1-2-6(9)5(3-4)8(10)11/h1-3,9H | | InChIKey | ZHRLVDHMIJDWSS-UHFFFAOYSA-N | | SMILES | C1(O)=CC=C(F)C=C1[N+]([O-])=O | | CAS DataBase Reference | 394-33-2(CAS DataBase Reference) | | NIST Chemistry Reference | 4-Fluoro-2-nitrophenol(394-33-2) | | EPA Substance Registry System | 4-Fluoro-2-nitrophenol (394-33-2) |
| Hazard Codes | Xn,Xi | | Risk Statements | 20/21/22-36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29089000 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Dermal Acute Tox. 4 Inhalation Acute Tox. 4 Oral Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| | 2-Nitro-4-fluorophenol Usage And Synthesis |
| Chemical Properties | yellow crystalline powder | | Uses | 4-Fluoro-2-nitrophenol may be used in the preparation of 5-fluoro-2-methoxyanilineand 5-fluoro-2-hydroxyaniline. | | General Description | 4-Fluoro-2-nitrophenol is formed during iron(III) nitrate nonahydrate activated by tungstophosphoric acid cesium salt catalyzed nitration of 4-fluorophenol. | | Synthesis | The general procedure for the synthesis of 2-nitro-4-fluorophenol from 4-fluorophenol was as follows: silica-loaded Al(NO3)3-9H2O (1 mmol) was added to a solution of 4-fluorophenol (1 mmol) in acetone (5 mL) and the reaction mixture was stirred at room temperature. The reaction process was monitored by TLC. Upon completion of the reaction, the reaction mixture was filtered and the silica residue was washed with ethyl acetate (25 mL). The filtrate and washings were combined and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (100-200 mesh) to give 2-nitro-4-fluorophenol (95%) and 4-nitro-4-fluorophenol (3%). | | References | [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1983, p. 75 - 82 [2] Synthetic Communications, 1997, vol. 27, # 19, p. 3301 - 3311 [3] Synlett, 2003, # 2, p. 191 - 194 [4] Synthetic Communications, 2005, vol. 35, # 2, p. 263 - 270 [5] Synthetic Communications, 1998, vol. 28, # 15, p. 2773 - 2781 |
| | 2-Nitro-4-fluorophenol Preparation Products And Raw materials |
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