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Atomfair Butenoic acid, 4,4,4-trifluoro-, ethyl ester C6H7F3O2
Description Ethyl 4,4,4-Trifluorobut-2-enoate (CAS No. 25597-16-4) is a high-purity fluorinated ester compound with the molecular formula C6H7F3O2. This specialized chemical is widely utilized in organic synthesis, pharmaceuticals, and material science due to its reactive trifluoromethyl group and ester functionality. The compound is characterized by its clear to pale-yellow liquid appearance, with a molecular weight of 168.12 g/mol and a boiling point of approximately 120-122??C. It is stored under inert conditions to maintain stability and purity, making it ideal for researchers requiring precise fluorinated building blocks. Suitable for nucleophilic addition, cross-coupling reactions, and polymer modifications, this ester is rigorously tested via…
Description
Description
Ethyl 4,4,4-Trifluorobut-2-enoate (CAS No. 25597-16-4) is a high-purity fluorinated ester compound with the molecular formula C6H7F3O2. This specialized chemical is widely utilized in organic synthesis, pharmaceuticals, and material science due to its reactive trifluoromethyl group and ester functionality. The compound is characterized by its clear to pale-yellow liquid appearance, with a molecular weight of 168.12 g/mol and a boiling point of approximately 120-122??C. It is stored under inert conditions to maintain stability and purity, making it ideal for researchers requiring precise fluorinated building blocks. Suitable for nucleophilic addition, cross-coupling reactions, and polymer modifications, this ester is rigorously tested via GC, NMR, and HPLC to ensure ??98% purity.
- CAS No: 25597-16-4
- Molecular Formula: C6H7F3O2
- Molecular Weight: 168.11
- Exact Mass: 168.03981395
- Monoisotopic Mass: 168.03981395
- IUPAC Name: ethyl 4,4,4-trifluorobut-2-enoate
- SMILES: CCOC(=O)C=CC(F)(F)F
- Synonyms: 406-10-0, Butenoic acid, 4,4,4-trifluoro-, ethyl ester, 2-BUTENOIC ACID, 4,4,4-TRIFLUORO-, ETHYL ESTER, ethyl 3-trifluoromethylacrylate, ethyl beta-trifluoromethylacrylate
Application
Ethyl 4,4,4-trifluorobut-2-enoate serves as a key intermediate in the synthesis of fluorinated pharmaceuticals, agrochemicals, and advanced polymers. Its trifluoromethyl group enhances metabolic stability and lipophilicity in drug design. Researchers employ it in Michael additions and Diels-Alder reactions to introduce fluorine motifs. The ester also acts as a monomer for specialty coatings with improved chemical resistance.
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