benzyl (3R)-3-(methylamino)pyrrolidine-1-carboxylate|917459-77-9,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)-

benzyl (3R)-3-(methylamino)pyrrolidine-1-carboxylate

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Chemical Name:	benzyl (3R)-3-(methylamino)pyrrolidine-1-carboxylate
CAS Number:	917459-77-9
Product Number:	AG00IGV0(AGN-PC-0OMXGD)
Synonyms:
MDL No:
Molecular Formula:	C13H18N2O2
Molecular Weight:	234.2942

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Chemical Structure

(R)-Benzyl 3-(methylamino)pyrrolidine-1-carboxylate is a versatile compound widely used in chemical synthesis. Its chirality and unique structure make it an essential building block in asymmetric synthesis, particularly in the production of pharmaceuticals and fine chemicals. This compound serves as a key intermediate in the preparation of various biologically active molecules due to its ability to introduce specific stereochemistry and functional groups into organic frameworks. By utilizing (R)-Benzyl 3-(methylamino)pyrrolidine-1-carboxylate, chemists can efficiently access a diverse range of enantiopure compounds with high selectivity, making it a valuable tool in the creation of complex molecular structures with precise control over stereochemistry.