Atomfair 2,2,2-Trifluoroethyl dimethylcarbamate C5H8F3NO2 CAS 407-43-2

Description

2,2,2-Trifluoroethyl dimethylcarbamate (CAS No. 407-43-2) is a high-purity specialty chemical with the molecular formula C₅H₈F₃NO₂. This compound, also known by its IUPAC name 2,2,2-trifluoroethyl N,N-dimethylcarbamate, is a fluorinated carbamate derivative designed for advanced research and industrial applications. Its unique trifluoroethyl group imparts distinct chemical properties, making it valuable in organic synthesis, pharmaceutical intermediates, and material science.

Our product is rigorously tested for purity and stability, ensuring consistent performance in demanding environments. Available in various quantities, it is supplied with comprehensive analytical documentation (including ¹H NMR, ¹³C NMR, and HPLC data) to meet stringent research requirements. Store in a cool, dry place under inert atmosphere for optimal shelf life.

Properties

• CAS Number: 407-43-2
• Complexity: 143
• IUPAC Name: 2,2,2-trifluoroethyl N,N-dimethylcarbamate
• InChI: InChI=1S/C5H8F3NO2/c1-9(2)4(10)11-3-5(6,7)8/h3H2,1-2H3
• InChI Key: ZZDGUXZHFOUZSO-UHFFFAOYSA-N
• Exact Mass: 171.05071298
• Molecular Formula: C5H8F3NO2
• Molecular Weight: 171.12
• SMILES: CN(C)C(=O)OCC(F)(F)F
• Topological: 29.5
• Monoisotopic Mass: 171.05071298
• Synonyms: 2,2,2-trifluoroethyl dimethylcarbamate, 407-43-2, 2,2,2-trifluoroethyl N,N-dimethylcarbamate, 2,2,2-TRIFLUOROETHYLDIMETHYLCARBAMATE, SCHEMBL2924441, DTXSID80572356, ZZDGUXZHFOUZSO-UHFFFAOYSA-N, MFCD08444253, AKOS009093809, AT40910, CS-0242064, EN300-24418, Dimethyl-carbamic acid 2,2,2-trifluoroethyl ester, Z196855268

Application

2,2,2-Trifluoroethyl dimethylcarbamate serves as a versatile building block in medicinal chemistry for the synthesis of fluorinated bioactive molecules. Its carbamate functionality enables use as a protecting group or precursor in peptide mimetics development. Researchers also employ it in materials science to modify polymer properties through fluorinated side-chain incorporation. The compound’s stability under acidic conditions makes it particularly useful for controlled-release formulations.

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