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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)-2-N-Cbz-aminomethylmorpholine

O=C(OCc1ccccc1)NC[C@@H]1CNCCO1 Request for Quotation
Chemical Name: (S)-2-N-Cbz-aminomethylmorpholine
CAS Number: 1174913-73-5
Product Number: AG000ED2(AGN-PC-0PAKN2)
Synonyms:
MDL No:
Molecular Formula: C13H18N2O3
Molecular Weight: 250.2936

Identification/Properties

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Chemical Structure


(S)-Benzyl (morpholin-2-ylmethyl)carbamate is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique structure, combining a benzyl group with a morpholine ring and a carbamate moiety, enables it to participate in a variety of reactions to synthesize complex molecules with high stereochemical control.One of the key applications of (S)-Benzyl (morpholin-2-ylmethyl)carbamate is in asymmetric synthesis, where it serves as a chiral auxiliary or a chiral ligand in catalytic reactions. By utilizing the chiral center provided by the carbamate group, this compound can induce asymmetry in chemical reactions, leading to the formation of enantiomerically pure products.Additionally, (S)-Benzyl (morpholin-2-ylmethyl)carbamate is often employed in the preparation of biologically active compounds and pharmaceutical intermediates. Its ability to introduce chirality in molecules makes it a valuable tool in the development of new drug candidates and fine chemicals.Furthermore, this compound can participate in various transformations such as asymmetric alkylations, reductions, and cycloadditions, expanding its utility in the synthesis of diverse chemical compounds. Its ease of modification and functional group tolerance make it a preferred choice for chemists looking to access enantiomerically enriched molecules efficiently.In summary, (S)-Benzyl (morpholin-2-ylmethyl)carbamate plays a crucial role in chemical synthesis by enabling the creation of chiral compounds with high selectivity. Its versatility and applications in asymmetric synthesis make it an indispensable tool for the preparation of complex molecules in both academic research and industrial settings.