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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)-tert-Butyl (3-(methoxymethyl)pyrrolidin-1-yl)carbamate

COC[C@H]1CCN(C1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: (S)-tert-Butyl (3-(methoxymethyl)pyrrolidin-1-yl)carbamate
CAS Number: 1421035-31-5
Product Number: AG00HWBT(AGN-PC-0WAH1Q)
Synonyms:
MDL No:
Molecular Formula: C11H22N2O3
Molecular Weight: 230.30398

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 (3-(methoxymethyl)pyrrolidin-1-yl)carbamate is a versatile compound frequently employed in chemical synthesis as a chiral building block. This compound plays a crucial role in asymmetric synthesis, allowing chemists to generate enantiomerically pure molecules with high stereoselectivity. Its unique structure and reactivity make it a valuable tool in the creation of complex organic compounds, particularly in the pharmaceutical and agrochemical industries. By incorporating (S)-tert-Butyl (3-(methoxymethyl)pyrrolidin-1-yl)carbamate into various synthetic routes, chemists can access a wide range of enantioselective reactions, facilitating the development of novel and biologically active molecules.