The chemical substance known as (2,3,4,5,6-pentafluorophenyl) 1-thieno[3,2-d]pyrimidin-4-ylpiperidine-4-carboxylate, with the CAS number 916766-92-2, is a complex organic compound characterized by its unique structural features. It contains a thieno[3,2-d]pyrimidine core, which is fused with a piperidine ring, and is further substituted with a pentafluorophenyl group and a carboxylate moiety. The presence of multiple fluorine atoms contributes to its lipophilicity and may enhance its biological activity, making it of interest in medicinal chemistry. The compound's structure suggests potential applications in pharmaceuticals, particularly in the development of targeted therapies. Its synthesis and characterization would typically involve advanced organic chemistry techniques, and its properties, such as solubility, stability, and reactivity, would be influenced by the electron-withdrawing nature of the fluorine substituents. Overall, this compound exemplifies the intricate design often found in drug discovery, where specific functional groups are strategically incorporated to optimize desired effects.

(2,3,4,5,6-pentafluorophenyl) 1-thieno[3,2-d]pyrimidin-4-ylpiperidine-4-carboxylate

916766-92-2: The chemical substance known as (2,3,4,5,6-pentafluorophenyl) 1-thieno[3,2-d]pyrimidin-4-ylpiperidine-4-carboxylate, with the CAS number 916766-92-2, is a complex organic compound characterized by its unique structural features. It contains a thieno[3,2-d]pyrimidine core, which is fused with a piperidine ring, and is further substituted with a pentafluorophenyl group and a carboxylate moiety. The presence of multiple fluorine atoms contributes to its lipophilicity and may enhance its biological activity, making it of interest in medicinal chemistry. The compound's structure suggests potential applications in pharmaceuticals, particularly in the development of targeted therapies. Its synthesis and characterization would typically involve advanced organic chemistry techniques, and its properties, such as solubility, stability, and reactivity, would be influenced by the electron-withdrawing nature of the fluorine substituents. Overall, this compound exemplifies the intricate design often found in drug discovery, where specific functional groups are strategically incorporated to optimize desired effects.

Pentafluorophenyl 1-(thieno[3,2-d]pyrimidin-4-yl)piperidine-4-carboxylate

CAS 916766-92-2

(2,3,4,5,6-pentafluorophenyl) 1-thieno[3,2-d]pyrimidin-4-ylpiperidine-4-carboxylate

Pentafluorophenyl 1-(thieno[3,2-d]pyrimidin-4-yl)piperidine-4-carboxylate

Ref: 54-PC8514