2-Deoxy-2,2-difluoro-4,5-O-(1-methylethylidene)-L-threo-pentonate acid, ethyl ester, is a synthetic organic compound characterized by its unique structural features, including the presence of difluoromethyl groups and an ethyl ester functional group. This compound belongs to the category of modified sugars, specifically pentonic acids, which are derivatives of pentose sugars. The difluoro substitution can enhance the compound's biological activity and stability, making it of interest in medicinal chemistry and pharmaceutical applications. The presence of the methylethylidene group contributes to its steric properties, potentially influencing its reactivity and interactions with biological targets. As with many fluorinated compounds, it may exhibit altered solubility and lipophilicity compared to its non-fluorinated counterparts. The compound's specific applications and behavior in biological systems would depend on further studies, including its synthesis, reactivity, and potential therapeutic uses. Safety and handling considerations are essential, particularly due to the presence of fluorine, which can impart unique toxicological properties.

2-DEOXY-2,2-DIFLUORO-4,5-O-(1-METHYLETHYLIDENE)-L-THREO-PENTONIC ACID, ETHYL ESTER

166376-98-3: 2-Deoxy-2,2-difluoro-4,5-O-(1-methylethylidene)-L-threo-pentonate acid, ethyl ester, is a synthetic organic compound characterized by its unique structural features, including the presence of difluoromethyl groups and an ethyl ester functional group. This compound belongs to the category of modified sugars, specifically pentonic acids, which are derivatives of pentose sugars. The difluoro substitution can enhance the compound's biological activity and stability, making it of interest in medicinal chemistry and pharmaceutical applications. The presence of the methylethylidene group contributes to its steric properties, potentially influencing its reactivity and interactions with biological targets. As with many fluorinated compounds, it may exhibit altered solubility and lipophilicity compared to its non-fluorinated counterparts. The compound's specific applications and behavior in biological systems would depend on further studies, including its synthesis, reactivity, and potential therapeutic uses. Safety and handling considerations are essential, particularly due to the presence of fluorine, which can impart unique toxicological properties.

CAS 166376-98-3

2-DEOXY-2,2-DIFLUORO-4,5-O-(1-METHYLETHYLIDENE)-L-THREO-PENTONIC ACID, ETHYL ESTER

(R)-Ethyl 3-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-difluoro-3-hydroxypropanoate

Ref: IN-DA001WO1

Gemcitabine Impurity 39

Ref: 4Z-G-2657