2,5-dioxo-1-[3-(pyridin-2-yldisulfanyl)propanoyloxy]pyrrolidine-3-sulfonic acid|121115-30-8,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,5-dioxo-1-[3-(pyridin-2-yldisulfanyl)propanoyloxy]pyrrolidine-3-sulfonic acid

O=S(C(C1)C(N(OC(CCSSC2=NC=CC=C2)=O)C1=O)=O)(O)=O

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Chemical Name:	2,5-dioxo-1-[3-(pyridin-2-yldisulfanyl)propanoyloxy]pyrrolidine-3-sulfonic acid
CAS Number:	121115-30-8
Product Number:	AG01FWMG(AGN-PC-01VIFJ)
Synonyms:
MDL No:
Molecular Formula:	C12H12N2O7S3
Molecular Weight:	392.43

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Chemical Structure

2,5-dioxo-1-(3-(pyridin-2-yldisulfanyl)propanoyloxy)pyrrolidine-3-sulfonic acid serves as a versatile reagent in chemical synthesis, particularly in the field of organic chemistry. This compound is widely utilized as a key building block for the synthesis of complex molecules with diverse applications.In chemical synthesis, 2,5-dioxo-1-(3-(pyridin-2-yldisulfanyl)propanoyloxy)pyrrolidine-3-sulfonic acid acts as a strategic intermediate in the formation of various pharmaceuticals, agrochemicals, and materials. Its unique structure containing both pyrrolidine and pyridine moieties allows for specific functionalization and manipulation, enabling chemists to access a wide range of target molecules.Furthermore, the sulfonic acid group present in the compound enhances its reactivity and solubility, making it a valuable tool in organic transformations such as esterification, amidation, and cross-coupling reactions. By incorporating 2,5-dioxo-1-(3-(pyridin-2-yldisulfanyl)propanoyloxy)pyrrolidine-3-sulfonic acid into synthesis routes, chemists can streamline their processes and access complex molecular architectures more efficiently.