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Atomfair Ethyl 2,2,2-trifluoroethyl oxalate C6H7F3O4
Description Ethyl 2,2,2-trifluoroethyl oxalate (CAS No. 1269151-38-3) is a high-purity fluorinated oxalate ester with the molecular formula C6H7F3O4. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique trifluoroethyl and oxalate functional groups. The compound is characterized by its excellent reactivity as a bifunctional building block, enabling the introduction of both ethyl and trifluoroethyl moieties in target molecules. It is supplied as a clear, colorless to pale yellow liquid with stringent quality control to ensure consistency in research applications. Suitable for use under inert conditions, this reagent is ideal for nucleophilic substitutions,…
Description
Description
Ethyl 2,2,2-trifluoroethyl oxalate (CAS No. 1269151-38-3) is a high-purity fluorinated oxalate ester with the molecular formula C6H7F3O4. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique trifluoroethyl and oxalate functional groups. The compound is characterized by its excellent reactivity as a bifunctional building block, enabling the introduction of both ethyl and trifluoroethyl moieties in target molecules. It is supplied as a clear, colorless to pale yellow liquid with stringent quality control to ensure consistency in research applications. Suitable for use under inert conditions, this reagent is ideal for nucleophilic substitutions, esterifications, and cross-coupling reactions. Store in a cool, dry place away from moisture and strong oxidizers to maintain stability.
- CAS No: 1269151-38-3
- Molecular Formula: C6H7F3O4
- Molecular Weight: 200.11
- Exact Mass: 200.02964319
- Monoisotopic Mass: 200.02964319
- IUPAC Name: 1-O-ethyl 2-O-(2,2,2-trifluoroethyl) oxalate
- SMILES: CCOC(=O)C(=O)OCC(F)(F)F
- Synonyms: ethyl 2,2,2-trifluoroethyl oxalate, 1269151-38-3, 1-O-ethyl 2-O-(2,2,2-trifluoroethyl) oxalate, ethyl?2,2,2-trifluoroethyl?oxalate, SCHEMBL18211788
Application
Ethyl 2,2,2-trifluoroethyl oxalate serves as a versatile intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its trifluoroethyl group enhances metabolic stability and bioavailability in drug candidates. Researchers employ this compound in the development of novel ligands and catalysts for asymmetric synthesis. Additionally, it is used in material science to modify polymer properties, such as thermal and chemical resistance. Its bifunctional nature allows for selective derivatization in complex molecular architectures.
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