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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)-

(S)-4,4-Dimethyl-5-oxopyrrolidine-2-carboxylic acid

OC(=O)[C@H]1NC(=O)C(C1)(C)C Request for Quotation
Chemical Name: (S)-4,4-Dimethyl-5-oxopyrrolidine-2-carboxylic acid
CAS Number: 1217832-12-6
Product Number: AG0015ZM(AGN-PC-0WAGDO)
Synonyms:
MDL No:
Molecular Formula: C7H11NO3
Molecular Weight: 157.1671

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, (S)-4,4-Dimethyl-5-oxopyrrolidine-2-carboxylic acid, also known as $name$, serves as a versatile building block for creating various compounds. This chiral compound plays a critical role in asymmetric synthesis, where the stereochemistry of the molecule influences the outcome of reactions. It can be used as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. With its unique structure, (S)-4,4-Dimethyl-5-oxopyrrolidine-2-carboxylic acid enables chemists to introduce chirality into molecules, leading to the formation of complex and highly functionalized products. Its applications extend to the synthesis of peptides, natural products, and fine chemicals, highlighting its significance in modern organic chemistry.