| CAS ID | 383-63-1 |
|---|---|
| IUPAC Name | ethyl 2,2,2-trifluoroacetate |
| Molecular Formula | C4H5F3O2 |
| Molecular Weight | |
| SMILES | CCOC(=O)C(F)(F)F |
| CAS ID | 383-63-1 |
|---|---|
| IUPAC Name | ethyl 2,2,2-trifluoroacetate |
| Molecular Formula | C4H5F3O2 |
| Molecular Weight | |
| SMILES | CCOC(=O)C(F)(F)F |
| 9794 |
Synonym : ethyl trifluoroacetate, trifluoroacetic acid ethyl ester, ethyltrifluoroacetate, acetic acid, trifluoro-, ethyl ester, trifluoroacetic acid, ethyl ester, ethyl trifluoroethanoate, unii-a6tzk6x11x, acetic acid, 2,2,2-trifluoro-, ethyl ester, a6tzk6x11x, ethyl ester of trifluoroacetic acid
| Boiling Point | 62°C |
| Color | Colorless |
| UN Number | 2924 |
| Formula Weight | 142.08 |
| Physical Form | Clear Liquid at 20°C |
| Chemical Name or Material | Ethyl Trifluoroacetate |
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Because it can engage in various organic processes, including esterifications and acylations, ethyl trifluoroacetate is frequently employed to synthesize medicines, agrochemicals, and other speciality chemicals.
The ethyl trifluoroacetate structure, with an ethyl group linked to the trifluoroacetate moiety, is highly reactive and stable, making it ideal for chemical synthesis and industrial uses.
Ethyl trifluoroacetate boiling point is around 105°C, indicating its volatility and appropriateness for reactions that need heat and regulated conditions.
The trifluoroacetic acid structure is composed of a carboxylic acid group (-COOH) coupled with a trifluoromethyl group (-CF3), which gives it distinct features such as high acidity and excellent solubility in polar liquids.
This compound's stable ethyl trifluoroacetate structure makes it very reactive in organic synthesis, allowing for selective acylation and generating a variety of fluorinated intermediates.
