The chemical substance known as 3-Pyridinecarboxylic acid, with the specified stereochemistry and structure, is a complex organic compound characterized by its multi-ring structure and various functional groups. It features a pyridine ring, which contributes to its aromatic properties, and a carboxylic acid group that imparts acidic characteristics. The presence of multiple stereocenters indicates that the compound can exist in different stereoisomeric forms, which may influence its biological activity and reactivity. The ester functional group suggests that it can undergo hydrolysis, leading to the release of the corresponding alcohol and acid. Additionally, the presence of a furan moiety indicates potential reactivity due to the unsaturation and oxygen atom in the ring. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its complex structure suggests that it could interact with biological systems in unique ways, potentially serving as a lead compound for drug development or as a tool in biochemical research.

3-Pyridinecarboxylicacid,(1R,2S,3R,4R,4aS,8aR)-4-[(1E)-2-(2,5-dihydro-5-oxo-3-furanyl)ethenyl]-1,2,3,4,4a,5,6,8a-octahydro-2,3-dihydroxy-3,4,8,8a-tetramethyl-1-naphthalenylester

1015776-92-7: The chemical substance known as 3-Pyridinecarboxylic acid, with the specified stereochemistry and structure, is a complex organic compound characterized by its multi-ring structure and various functional groups. It features a pyridine ring, which contributes to its aromatic properties, and a carboxylic acid group that imparts acidic characteristics. The presence of multiple stereocenters indicates that the compound can exist in different stereoisomeric forms, which may influence its biological activity and reactivity. The ester functional group suggests that it can undergo hydrolysis, leading to the release of the corresponding alcohol and acid. Additionally, the presence of a furan moiety indicates potential reactivity due to the unsaturation and oxygen atom in the ring. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its complex structure suggests that it could interact with biological systems in unique ways, potentially serving as a lead compound for drug development or as a tool in biochemical research.

<p>6-O-Nicotinoylbarbatin C is a natural product</p>

CAS 1015776-92-7

3-Pyridinecarboxylicacid,(1R,2S,3R,4R,4aS,8aR)-4-[(1E)-2-(2,5-dihydro-5-oxo-3-furanyl)ethenyl]-1,2,3,4,4a,5,6,8a-octahydro-2,3-dihydroxy-3,4,8,8a-tetramethyl-1-naphthalenylester

6-O-Nicotinoylbarbatin C

Ref: TM-TN1323