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Sigma Aldrich Ethyl 4,4,4-trifluoroacetoacetate
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Description
- Ethyl 4,4,4-trifluoroacetoacetate (etfaa) is a general reagent to synthesize enantiopure trifluoromethyl-functionalized products. applications include:
- Synthesis of (s)- and (r)-α-trifluoromethyl-aspartic acid and α- trifluoromethyl-serine from chiral cf3-oxazolidines, which is derived from etfaa
- Enantiopure synthesis of trifluoromethyl-α-amino acid derivatives
- Synthesis of (2r)-2-trifluoromethyl-2-carboxyazetidine, (r)- and (s)-trifluoromethylhomoserines from oxazolidine intermediate obtained by condensing (r)-phenylglycinol with etfaa
Specifications
Specifications
| CAS | 372-31-6 |
| Density | 1.259 g/mL (at 25°C (literature)) |
| Boiling Point | 129°C to 130°C (lit.) |
| Molecular Formula | C6H7F3O3 |
| Refractive Index | n20/D 1.375 (literature) |
| Linear Formula | CF3COCH2CO2C2H5 |
| MDL Number | MFCD00000424 |
| Quantity | 100 g |
| Synonym | ETFAA; Ethyl 3-oxo-4,4,4-trifluorobutyrate |
| Molecular Weight (g/mol) | 184.11 |
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