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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)-

2-Pyrrolidinone, 1-methyl-5-(1-oxido-3-pyridinyl)-, (5S)-

[O-][n+]1cccc(c1)C1CCC(=O)N1C Request for Quotation
Chemical Name: 2-Pyrrolidinone, 1-methyl-5-(1-oxido-3-pyridinyl)-, (5S)-
CAS Number: 36508-80-2
Product Number: AG0079OB(AGN-PC-0O9CRB)
Synonyms:
MDL No:
Molecular Formula: C10H12N2O2
Molecular Weight: 192.2145

Identification/Properties

Computed Properties
Molecular Weight:
192.218g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
192.09g/mol
Monoisotopic Mass:
192.09g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
232
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-3-(1-Methyl-5-oxopyrrolidin-2-yl)pyridine 1-oxide, commonly known as $name$, is a versatile reagent widely utilized in chemical synthesis. This compound serves as a key intermediate in various organic reactions, particularly in the production of pharmaceutical compounds and fine chemicals. One important application of $name$ in chemical synthesis is its role as a chiral building block. Due to its unique structure and stereochemistry, (S)-3-(1-Methyl-5-oxopyrrolidin-2-yl)pyridine 1-oxide can be employed to introduce chirality into molecules, enabling the creation of enantiomerically pure products. This is crucial in the pharmaceutical industry, where the stereochemistry of a compound can significantly impact its biological activity and efficacy.Furthermore, (S)-3-(1-Methyl-5-oxopyrrolidin-2-yl)pyridine 1-oxide can participate in a variety of chemical transformations, such as nucleophilic addition reactions, asymmetric hydrogenation, and metal-catalyzed coupling reactions. Its versatility and ability to selectively influence the stereochemistry of the products make it a valuable tool for synthetic chemists working on complex molecule synthesis.In conclusion, the application of (S)-3-(1-Methyl-5-oxopyrrolidin-2-yl)pyridine 1-oxide in chemical synthesis offers a pathway to efficient, selective, and enantioselective synthesis of important compounds, making it a valuable reagent in the toolkit of synthetic chemists.