2-[[(3α,5β,7β)-3,7-Dihydroxy-24-oxocholan-24-yl]amino]ethanesulfonic acid, also known as Chenodeoxycholyltaurine, serves a crucial role in chemical synthesis as a versatile building block and reactive intermediate. Its unique structure, derived from bile acid conjugation, offers a wide range of applications in organic synthesis. In chemical synthesis, Chenodeoxycholyltaurine can be utilized as a chiral resolving agent due to the presence of the hydroxyl groups on the steroid ring, enabling enantioselective transformations. Additionally, its sulfonic acid moiety imparts water solubility, facilitating its use in aqueous reactions and as a phase-transfer catalyst.Furthermore, Chenodeoxycholyltaurine can be employed as a protecting group for amino functions, allowing for selective derivatization and manipulation of amino acids and peptides. Its inclusion in complex molecule synthesis enhances efficiency and selectivity, particularly in the formation of peptide bonds and steroidal derivatives.Overall, the incorporation of 2-[[(3α,5β,7β)-3,7-Dihydroxy-24-oxocholan-24-yl]amino]ethanesulfonic acid in chemical synthesis enables the construction of diverse compounds with structural complexity and biological relevance.
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