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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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)-

L-Proline, 5-oxo-1-(phenylmethyl)-, 1,1-dimethylethyl ester

O=C([C@@H]1CCC(=O)N1Cc1ccccc1)OC(C)(C)C Request for Quotation
Chemical Name: L-Proline, 5-oxo-1-(phenylmethyl)-, 1,1-dimethylethyl ester
CAS Number: 90741-27-8
Product Number: AG0039VJ(AGN-PC-0OMFQ5)
Synonyms:
MDL No:
Molecular Formula: C16H21NO3
Molecular Weight: 275.3428

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-tert-Butyl 1-benzyl-5-oxopyrrolidine-2-carboxylate is a versatile compound that finds key applications in chemical synthesis, particularly in the realm of asymmetric synthesis. This chiral compound serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to introduce chirality into molecules with high enantioselectivity.In chemical synthesis, (S)-tert-Butyl 1-benzyl-5-oxopyrrolidine-2-carboxylate acts as a chiral auxiliary, facilitating the creation of enantiomerically pure compounds. It can be used in a range of reactions such as asymmetric aldol reactions, Michael additions, hydrogenations, and cycloadditions to produce single enantiomer products with high optical purity. Incorporating this compound into synthetic pathways enables chemists to access a wide array of chiral molecules that are crucial in drug discovery and development.Moreover, the stereochemistry imparted by (S)-tert-Butyl 1-benzyl-5-oxopyrrolidine-2-carboxylate can significantly influence the biological activity and properties of synthesized compounds, making it an indispensable tool in the design and production of new chemical entities. Its ability to control the stereochemical outcome of reactions makes it a valuable asset in the quest for developing more efficient and selective chemical processes in various industries.