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| | Ethyl trifluoropyruvate Basic information |
| Product Name: | Ethyl trifluoropyruvate | | Synonyms: | Ethyl trifluoropyruvate, Ethyl 2-oxo-3,3,3-trifluoropropionate;Threefluorideethylpyruvate;Ethyl 3,3,3-trifluoropyruvate 97%;ETHYL TRIFLUOROPYRUVATE;ETHYL 2-OXO-3,3,3-TRIFLUORO PROPIONATE;E-TFPA;3,3,3-TRIFLUORO-2-OXOPROPANOIC ACID ETHYL ESTER;RARECHEM AL BI 1300 | | CAS: | 13081-18-0 | | MF: | C5H5F3O3 | | MW: | 170.09 | | EINECS: | 603-440-7 | | Product Categories: | C2 to C5;Carbonyl Compounds;Esters | | Mol File: | 13081-18-0.mol |  |
| | Ethyl trifluoropyruvate Chemical Properties |
| Boiling point | 42 °C(lit.) | | density | 1.283 g/mL at 25 °C (lit.) | | vapor pressure | 12.49hPa at 25℃ | | refractive index | n20/D 1.341(lit.) | | Fp | 88 °F | | storage temp. | Inert atmosphere,2-8°C | | solubility | Miscible with dichloromethane. | | form | Liquid | | color | Clear colorless to pale yellow | | BRN | 2087388 | | Stability: | Moisture Sensitive | | InChIKey | KJHQVUNUOIEYSV-UHFFFAOYSA-N | | LogP | -0.05 | | CAS DataBase Reference | 13081-18-0(CAS DataBase Reference) |
| Hazard Codes | Xn,C,Xi | | Risk Statements | 10-22-36/37/38 | | Safety Statements | 26-37/39-16 | | RIDADR | UN 3272 3/PG 3 | | WGK Germany | 3 | | Hazard Note | Corrosive | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29183000 |
| | Ethyl trifluoropyruvate Usage And Synthesis |
| Chemical Properties | Clear pale yellow liquid | | Uses | Ethyl 3,3,3-trifluoropyruvate may be used in the preparation of N-heteroaryl(trifluoromethyl)hydroxyalkanoic acid esters. | | Uses | Ethyl trifluoropyruvate acts as a building block in synthetic chemistry for the synthesis of fluorine containing compounds. It is also used as a reagent for the preparation of potential biologically active compounds like highly enantioselective organocatalytic hydroxyalkylation of indoles. | | Uses | Ethyl Trifluoropyruvate is used as a reagent in the preparation of potential biologically active compounds such as in the highly enantioselective organocatalytic hydroxyalkylation of indoles .
| | General Description | Ethyl 3,3,3-trifluoropyruvate is a trifluoromethylated compound. Enantioselective Friedel–Crafts alkylation of simple phenols and indoles with ethyl 3,3,3-trifluoropyruvate under different reaction conditions have been reported. |
| | Ethyl trifluoropyruvate Preparation Products And Raw materials |
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