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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)-N-Boc-2-(2-hydroxyethyl)morpholine

OCC[C@@H]1OCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: (S)-N-Boc-2-(2-hydroxyethyl)morpholine
CAS Number: 1257856-15-7
Product Number: AG000OPZ(AGN-PC-0O0R2B)
Synonyms:
MDL No:
Molecular Formula: C11H21NO4
Molecular Weight: 231.2887

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-N-Boc-2-(2-Hydroxyethyl)morpholine is a versatile compound commonly utilized in chemical synthesis for its ability to serve as a chiral building block. With its unique molecular structure, this compound plays a crucial role in the creation of enantiomerically pure pharmaceuticals, agrochemicals, and other complex organic molecules. In asymmetric synthesis, (S)-N-Boc-2-(2-Hydroxyethyl)morpholine acts as a key intermediate, allowing chemists to introduce chirality efficiently and control the stereochemistry of the final product. Its incorporation into various synthetic pathways enables the production of enantioenriched compounds with high stereochemical purity, making it a valuable tool in the development of cutting-edge materials and biologically active compounds. Furthermore, the hydroxyethyl group in the molecule offers additional reactivity and opportunities for functionalization, expanding the range of potential applications in the field of organic chemistry.