Description

Discover the precision and purity of (3R,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyldihydrofuran-2(3H)-one (CAS No. 879551-04-9), a highly specialized fluorinated lactone derivative designed for advanced research and pharmaceutical applications. With a molecular formula of C6H9FO4, this compound exhibits exceptional stereochemical purity, making it a critical intermediate in the synthesis of nucleoside analogs and other bioactive molecules. Our product is rigorously tested for quality, ensuring ≥95% purity via HPLC, and is available in various quantities to meet your laboratory needs. Ideal for medicinal chemistry, enzymology studies, and drug discovery, this compound is packaged under inert conditions to guarantee stability and longevity.

Properties

• CAS Number: 879551-04-9
• Complexity: 183
• IUPAC Name: (3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyl-tetrahydrofuran-2-one
• InChI: InChI=1S/C6H9FO4/c1-6(7)4(9)3(2-8)11-5(6)10/h3-4,8-9H,2H2,1H3/t3-,4-,6-/m1/s1
• InChI Key: VNCJYMKHJWVTPK-ZMIZWQJLSA-N
• Exact Mass: 164.04848693
• Molecular Formula: C6H9FO4
• Molecular Weight: 164.13
• SMILES: C[C@]1([C@@H]([C@H](OC1=O)CO)O)F
• Topological: 66.8
• Monoisotopic Mass: 164.04848693
• Synonyms: 879551-04-9, (3R,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyldihydrofuran-2(3H)-one, (3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyloxolan-2-one, (3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxyMethyl)-3-Methyl-dihydrofuran-2(3H)-one, 2-deoxy-2-fluoro-2-c-methyl-d-ribono-1,4-lactone, MFCD23106443, VNCJYMKHJWVTPK-ZMIZWQJLSA-N, SCHEMBL768087, DTXSID60718033, BCP11287, AKOS025290711, MF44944, PB37368, AS-43164, CS-0009690, 3-fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyloxolan-2-one, D-erythro-Pentonic acid, 2-deoxy-2-fluoro-2-methyl-, gamma-lactone, (2R) -2-Deoxy-2-fluoro-2-methyl-D- erythro- pentonic acid gamma-lactone;2- Deoxy- 2- fluoro- 2- C- methyl- d- ribono- gamma- lactone ;(3R,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyl-dihydrofuran-2(3H)-one

This fluorinated lactone derivative serves as a key intermediate in the synthesis of modified nucleosides, particularly in the development of antiviral and anticancer agents. Its unique stereochemistry enables precise modulation of biological activity, making it valuable for structure-activity relationship (SAR) studies. Researchers also utilize it in enzymatic assays to investigate fluorinated sugar metabolism. Its stability and reactivity profile make it suitable for click chemistry and other advanced synthetic applications.

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