Ethyl 2-deoxy-2,2-difluoro-4,5-O-(1-methylethylidene)-D-threo-pentonate, with the CAS number 95058-93-8, is a chemical compound characterized by its unique structural features, including the presence of difluoro and methylethylidene groups. This compound is a derivative of a pentose sugar, specifically a D-threo configuration, which influences its stereochemistry and biological activity. The ethyl ester functional group contributes to its solubility and reactivity, making it potentially useful in various chemical reactions or as an intermediate in organic synthesis. The difluoro substitution may enhance its stability and alter its interaction with biological systems, potentially impacting its pharmacological properties. As with many fluorinated compounds, it may exhibit unique characteristics such as increased lipophilicity or altered metabolic pathways. Overall, the specific properties and applications of this compound would depend on further experimental studies and characterization techniques, including NMR, IR spectroscopy, and mass spectrometry, to elucidate its behavior in different environments.

ethyl 2-deoxy-2,2-difluoro-4,5-O-(1-methylethylidene)-D-threo-pentonate

95058-93-8: Ethyl 2-deoxy-2,2-difluoro-4,5-O-(1-methylethylidene)-D-threo-pentonate, with the CAS number 95058-93-8, is a chemical compound characterized by its unique structural features, including the presence of difluoro and methylethylidene groups. This compound is a derivative of a pentose sugar, specifically a D-threo configuration, which influences its stereochemistry and biological activity. The ethyl ester functional group contributes to its solubility and reactivity, making it potentially useful in various chemical reactions or as an intermediate in organic synthesis. The difluoro substitution may enhance its stability and alter its interaction with biological systems, potentially impacting its pharmacological properties. As with many fluorinated compounds, it may exhibit unique characteristics such as increased lipophilicity or altered metabolic pathways. Overall, the specific properties and applications of this compound would depend on further experimental studies and characterization techniques, including NMR, IR spectroscopy, and mass spectrometry, to elucidate its behavior in different environments.

CAS 95058-93-8

ethyl 2-deoxy-2,2-difluoro-4,5-O-(1-methylethylidene)-D-threo-pentonate

Gemcitabine Impurity 34

Ref: 4Z-G-2652

2-Deoxy-2,2-difluoro-4,5-O-isopropylidene-D-threo-pentonic Acid Ethyl Ester

Ref: TR-D232830