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Atomfair Methyl (2R)-2-fluoropropanoate C4H7FO2

Description Methyl (2R)-2-fluoropropanoate (CAS No. 146805-74-5) is a high-purity chiral fluorinated ester with the molecular formula C4H7FO2. This compound is a valuable building block in organic synthesis and pharmaceutical research, particularly for the introduction of fluorine atoms into target molecules. Its (R)-enantiomeric form ensures stereochemical precision, making it ideal for asymmetric synthesis and the development of bioactive compounds. The product is rigorously tested for purity and stability, ensuring reliable performance in sensitive applications. Packaged under inert conditions to prevent degradation, it is suitable for use in medicinal chemistry, agrochemical research, and material science.

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Description

Description

Methyl (2R)-2-fluoropropanoate (CAS No. 146805-74-5) is a high-purity chiral fluorinated ester with the molecular formula C4H7FO2. This compound is a valuable building block in organic synthesis and pharmaceutical research, particularly for the introduction of fluorine atoms into target molecules. Its (R)-enantiomeric form ensures stereochemical precision, making it ideal for asymmetric synthesis and the development of bioactive compounds. The product is rigorously tested for purity and stability, ensuring reliable performance in sensitive applications. Packaged under inert conditions to prevent degradation, it is suitable for use in medicinal chemistry, agrochemical research, and material science.

  • CAS No: 146805-74-5
  • Molecular Formula: C4H7FO2
  • Molecular Weight: 106.10
  • Exact Mass: 106.04300762
  • Monoisotopic Mass: 106.04300762
  • IUPAC Name: methyl (2R)-2-fluoropropanoate
  • SMILES: C[C@H](C(=O)OC)F
  • Synonyms: methyl (2r)-2-fluoropropanoate, 478-990-2, (r)-methyl 2-fluoropropionate, 146805-74-5, methyl (r)-2-fluoropropionate

Application

Methyl (2R)-2-fluoropropanoate is widely used as a chiral synthon in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its stereospecificity makes it valuable for constructing enantiomerically pure compounds with enhanced biological activity. Researchers utilize this ester in nucleophilic fluorination reactions and as a precursor for fluorinated amino acids. It is also employed in the development of PET radiotracers and other diagnostic agents.

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