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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)-

(R)-TERT-BUTYL-2-(2-HYDROXYETHYL)MORPHOLINE-4-CARBOXYLATE

OCC[C@H]1OCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: (R)-TERT-BUTYL-2-(2-HYDROXYETHYL)MORPHOLINE-4-CARBOXYLATE
CAS Number: 136992-21-7
Product Number: AG0012N3(AGN-PC-0O1BNS)
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 (R)-tert-Butyl 2-(2-hydroxyethyl)morpholine-4-carboxylate is a valuable compound widely used in chemical synthesis as a chiral building block. Its unique structure containing a morpholine ring and a hydroxyethyl group makes it a versatile tool in asymmetric synthesis. This compound is particularly significant in the development of pharmaceuticals, agrochemicals, and advanced materials due to its ability to introduce chirality with high efficiency and selectivity. In addition, (R)-tert-Butyl 2-(2-hydroxyethyl)morpholine-4-carboxylate serves as a key intermediate in the synthesis of various bioactive compounds and complex molecules, enabling the creation of diverse chemical structures with specific stereochemical properties. Its role in catalysis and stereoselective transformations make it an essential component in the modern toolbox of organic chemists striving to access enantiopure compounds for a range of applications.