Methyl (3S,4S,5S,6S)-3,4,5-triacetoxy-6-(4-iodophenoxy)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 compound features a 4-iodophenoxy substituent, which introduces both an aromatic character and a halogen, potentially influencing its biological activity and solubility. The stereochemistry is defined by the (3S,4S,5S,6S) configuration, indicating specific spatial arrangements of the substituents around the chiral centers, which can affect the compound's interactions with biological systems. This compound may exhibit properties such as being a potential intermediate in organic synthesis or having pharmacological relevance due to its structural features. Its CAS number, 490028-18-7, allows for precise identification in chemical databases, facilitating research and application in various fields, including medicinal chemistry and materials science.

methyl (3S,4S,5S,6S)-3,4,5-triacetoxy-6-(4-iodophenoxy)tetrahydropyran-2-carboxylate

490028-18-7: Methyl (3S,4S,5S,6S)-3,4,5-triacetoxy-6-(4-iodophenoxy)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 compound features a 4-iodophenoxy substituent, which introduces both an aromatic character and a halogen, potentially influencing its biological activity and solubility. The stereochemistry is defined by the (3S,4S,5S,6S) configuration, indicating specific spatial arrangements of the substituents around the chiral centers, which can affect the compound's interactions with biological systems. This compound may exhibit properties such as being a potential intermediate in organic synthesis or having pharmacological relevance due to its structural features. Its CAS number, 490028-18-7, allows for precise identification in chemical databases, facilitating research and application in various fields, including medicinal chemistry and materials science.

<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 490028-18-7

methyl (3S,4S,5S,6S)-3,4,5-triacetoxy-6-(4-iodophenoxy)tetrahydropyran-2-carboxylate

4-Iodophenyl 2,3,4-Tri-O-acetyl-β-D-glucuronide Methyl Ester

Ref: TR-I718770