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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)-

Carbamic acid, [(3S)-2-oxo-3-pyrrolidinyl]-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)N[C@H]1CCNC1=O Request for Quotation
Chemical Name: Carbamic acid, [(3S)-2-oxo-3-pyrrolidinyl]-, 1,1-dimethylethyl ester
CAS Number: 92235-34-2
Product Number: AG0036Q1(AGN-PC-0ON57B)
Synonyms:
MDL No:
Molecular Formula: C9H16N2O3
Molecular Weight: 200.2349

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
200.238g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
200.116g/mol
Monoisotopic Mass:
200.116g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
245
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
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)-tert-Butyl (2-oxopyrrolidin-3-yl)carbamate is a versatile intermediate in chemical synthesis widely utilized for its chiral properties. This compound serves as a key building block in organic chemistry, specifically in the development of pharmaceuticals, agrochemicals, and materials science.Its unique structural configuration imparts stereochemical control, making it invaluable in asymmetric synthesis strategies. The (S)-tert-Butyl (2-oxopyrrolidin-3-yl)carbamate moiety is known for its ability to act as a chiral auxiliary or a chiral ligand in various transformations, facilitating the formation of enantiomerically pure compounds.In addition, this compound can be employed in the synthesis of complex molecules such as natural products and bioactive compounds where precise stereochemistry is essential. Its compatibility with a wide range of synthetic methodologies further enhances its utility in organic synthesis, enabling chemists to access a diverse array of structurally diverse molecules efficiently and selectively.