(S)-5-Oxopyrrolidine-2-carboxylic acid benzyl ester|94885-52-6,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)-

(S)-5-Oxopyrrolidine-2-carboxylic acid benzyl ester

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Chemical Name:	(S)-5-Oxopyrrolidine-2-carboxylic acid benzyl ester
CAS Number:	94885-52-6
Product Number:	AG00IIMU(AGN-00IIHA)
Synonyms:
MDL No:
Molecular Formula:	C12H13NO3
Molecular Weight:	219.2365

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Chemical Structure

(S)-5-Oxopyrrolidine-2-carboxylic acid benzyl ester, a versatile chemical compound, finds extensive application in chemical synthesis as a key intermediate for the production of pharmaceuticals, agrochemicals, and functional materials. This compound serves as a crucial building block in the synthesis of various complex molecules due to its unique structural characteristics and reactivity. By selectively manipulating the functional groups present in this compound, chemists can easily incorporate it into multi-step synthesis routes to develop a wide range of bioactive compounds, such as enzyme inhibitors, pharmaceutical drugs, and biologically active molecules. Additionally, (S)-5-Oxopyrrolidine-2-carboxylic acid benzyl ester plays a significant role in the development of novel materials with tailored properties for applications in fields like medicine, agriculture, and materials science. By leveraging its chemical properties and reactivity, researchers can efficiently access diverse chemical space and innovate new molecules with enhanced functionalities and potential industrial applications.