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| | 1,1,1-Trifluoro-4-iodobutane Basic information |
| Product Name: | 1,1,1-Trifluoro-4-iodobutane | | Synonyms: | 1-IODO-4,4,4-TRIFLUOROBUTANE;1,1,1-TRIFLUORO-4-IODOBUTANE;4,4,4-TRIFLUORO-1-IODOBUTANE;4,4,4-TRIFLUOROBUTYL IODIDE;4-IODO-1,1,1-TRIFLUOROBUTANE;1-Iodo-4,4,4-trifluorobutane 99%;1-Iodo-4,4,4-trifluorobutane99%;1-IODO-4,4,4-TRIFLUOROBUTANE, 98+% | | CAS: | 461-17-6 | | MF: | C4H6F3I | | MW: | 237.99 | | EINECS: | | | Product Categories: | | | Mol File: | 461-17-6.mol |  |
| | 1,1,1-Trifluoro-4-iodobutane Chemical Properties |
| Boiling point | 126 °C | | density | 1.85 | | refractive index | 1.4326 | | Fp | >100°C | | storage temp. | 2-8°C(protect from light) | | form | clear liquid | | color | Colorless to Light yellow to Light orange | | Sensitive | Light Sensitive | | BRN | 1736064 | | InChI | InChI=1S/C4H6F3I/c5-4(6,7)2-1-3-8/h1-3H2 | | InChIKey | LNDGACQEAYKNOI-UHFFFAOYSA-N | | SMILES | C(F)(F)(F)CCCI | | CAS DataBase Reference | 461-17-6(CAS DataBase Reference) |
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ALFA
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| | 1,1,1-Trifluoro-4-iodobutane Usage And Synthesis |
| Description | 1,1,1-Trifluoro-4-iodobutane is an organic compound with the chemical formula CIF3. It is a colorless liquid that reacts with water and alcohol to form hydrogen fluoride and hydrofluoric acid. 1,1,1-Trifluoro-4-iodobutane is a potent sensitizer that can irritate the skin and eyes. It has been used experimentally as a solvent for diethyl ether in the synthesis of piperidinium salts. The cavity viscosity of 1,1,1-trifluoro-4-iodobutane has been measured at room temperature and found to be 0.0038 Pa·s at 25 °C. In laboratory tests, this molecule has shown antibacterial activity against Propionibacterium acnes (P. acnes) and Staphylococcus aureus (S. aureus). | | Uses | 1,1,1-Trifluoro-4-Iodobutane can be used to prepare small molecule inhibitors of SLC15A4 possessing anti-inflammatory activity. | | Synthesis | In a 1.0 L reactor add 0.8 g of 18-crown-6, 3 mol of CF3CH2CH2CH2Cl, 1.5 mol of potassium iodide and
After 500 ml of acetone, the reactor was sealed. With stirring on, the reactor was warmed up to 90 C and reacted at a constant temperature for 6
h. The reactants were filtered and distilled to give CF3CH2CH2CH2CH2I in 93.4% yield based on potassium iodide. |
| | 1,1,1-Trifluoro-4-iodobutane Preparation Products And Raw materials |
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