Methyl (3R,4R,5R,6R)-3,4,5-triacetoxy-6-(3-acetoxy-5-iodo-phenoxy)tetrahydropyran-2-carboxylate is a complex organic compound characterized by its tetrahydropyran ring structure, which is a six-membered cyclic ether. The presence of multiple acetoxy groups indicates that it has significant reactivity and potential for further chemical modifications. The iodo-substituted phenoxy group suggests that this compound may exhibit unique biological activities, possibly related to its iodine content, which can enhance lipophilicity and influence pharmacokinetics. The stereochemistry denoted by the (3R,4R,5R,6R) configuration indicates that the compound has specific spatial arrangements that can affect its interaction with biological targets. This compound is likely to be soluble in organic solvents due to its ester and ether functionalities, while its polar groups may impart some degree of solubility in polar solvents. Overall, this compound's structural complexity and functional groups suggest potential applications in medicinal chemistry and organic synthesis.

methyl (3R,4R,5R,6R)-3,4,5-triacetoxy-6-(3-acetoxy-5-iodo-phenoxy)tetrahydropyran-2-carboxylate

490028-21-2: Methyl (3R,4R,5R,6R)-3,4,5-triacetoxy-6-(3-acetoxy-5-iodo-phenoxy)tetrahydropyran-2-carboxylate is a complex organic compound characterized by its tetrahydropyran ring structure, which is a six-membered cyclic ether. The presence of multiple acetoxy groups indicates that it has significant reactivity and potential for further chemical modifications. The iodo-substituted phenoxy group suggests that this compound may exhibit unique biological activities, possibly related to its iodine content, which can enhance lipophilicity and influence pharmacokinetics. The stereochemistry denoted by the (3R,4R,5R,6R) configuration indicates that the compound has specific spatial arrangements that can affect its interaction with biological targets. This compound is likely to be soluble in organic solvents due to its ester and ether functionalities, while its polar groups may impart some degree of solubility in polar solvents. Overall, this compound's structural complexity and functional groups suggest potential applications in medicinal chemistry and organic synthesis.

<p>Applications Intermediate for the synthesis of glucuronide conjugates of trans-Resveratrol<br>References Learmonth, D.A., et al.: Bioconjug. Chem., 14, 262 (2003),<br></p>

CAS 490028-21-2

methyl (3R,4R,5R,6R)-3,4,5-triacetoxy-6-(3-acetoxy-5-iodo-phenoxy)tetrahydropyran-2-carboxylate

3-(Acetyloxy)-5-iodophenol-2’,3’,4’-tri-O-acetyl-β-D-glucuronide Methyl Ester

Ref: TR-A166000