114869-83-9 | β-D-Glucopyranosiduronic acid, 2-(9H-carbazol-4-yloxy)-1-[[[2-(2-methoxyphenoxy)ethyl]amino]methyl]ethyl

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Description

• Catalog Number: AA19705
• Chemical Name: β-D-Glucopyranosiduronic acid, 2-(9H-carbazol-4-yloxy)-1-[[[2-(2-methoxyphenoxy)ethyl]amino]methyl]ethyl
• CAS Number: 114869-83-9
• Molecular Formula: C30H34N2O10
• Molecular Weight: 582.5984
• MDL Number: MFCD23160274
• SMILES: COc1ccccc1OCCNCC(O[C@@H]1O[C@H](C(=O)O)[C@H]([C@@H]([C@H]1O)O)O)COc1cccc2c1c1ccccc1[nH]2

Upstream Synthesis Route

Carvedilol β-D-Glucuronide, the mixture of diastereomers, is a valuable compound in chemical synthesis due to its unique properties and applications. One significant use of this compound is as a chiral building block in the synthesis of pharmaceutical intermediates. Its diastereomeric nature allows for selective transformations that lead to the creation of new chiral centers with high enantioselectivity.Additionally, Carvedilol β-D-Glucuronide can serve as a versatile protecting group in the protection-deprotection strategies commonly employed in organic synthesis. Its ability to undergo selective transformations under mild conditions makes it a valuable tool for the synthesis of complex molecules. By strategically incorporating this compound into synthetic pathways, chemists can efficiently access a wide range of structurally diverse molecules with high stereocontrol.Furthermore, the presence of the glucuronide moiety in Carvedilol β-D-Glucuronide can facilitate the purification and isolation of intermediates during the synthesis process. This property streamlines the synthetic workflow and enhances the overall efficiency of the chemical synthesis.In conclusion, Carvedilol β-D-Glucuronide, as a mixture of diastereomers, plays a crucial role in modern chemical synthesis by enabling selective transformations, serving as a chiral building block, and facilitating purification processes. Its utility and versatility make it a valuable asset in the toolbox of synthetic chemists seeking to access complex and stereochemically diverse molecules.