Chemical Name: | (S)-3-(Toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid benzyl ester |
CAS Number: | 158654-83-2 |
Product Number: | AG001QPZ(AGN-PC-0WA2Y2) |
Synonyms: | |
MDL No: | |
Molecular Formula: | C19H21NO5S |
Molecular Weight: | 375.4387 |
(S)-Benzyl 3-(tosyloxy)pyrrolidine-1-carboxylate is a versatile compound widely employed in chemical synthesis for its unique structural properties. This compound serves as a crucial building block in organic synthesis, particularly in the formation of various nitrogen-containing molecules.One key application of (S)-Benzyl 3-(tosyloxy)pyrrolidine-1-carboxylate is its role as a chiral auxiliary in asymmetric synthesis. By utilizing this compound, chemists can introduce chirality into target molecules, enabling the production of enantiopure compounds with high optical purity. This is especially valuable in pharmaceutical and agrochemical industries, where the biological activity of a molecule is often dependent on its stereochemistry.Furthermore, (S)-Benzyl 3-(tosyloxy)pyrrolidine-1-carboxylate can be utilized in the synthesis of various alkaloid derivatives and other heterocyclic compounds. Its ability to undergo selective transformations under mild reaction conditions makes it a valuable precursor for the preparation of complex organic molecules.In summary, the application of (S)-Benzyl 3-(tosyloxy)pyrrolidine-1-carboxylate in chemical synthesis extends to asymmetric synthesis, chiral molecule preparation, and the construction of nitrogen-containing organic frameworks, making it an indispensable tool for synthetic chemists seeking to access a diverse range of structurally diverse compounds.