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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)-

3-Morpholineethanol, (3S)-

OCC[C@H]1COCCN1 Request for Quotation
Chemical Name: 3-Morpholineethanol, (3S)-
CAS Number: 761460-05-3
Product Number: AG005ROS(AGN-PC-0OHRSY)
Synonyms:
MDL No:
Molecular Formula: C6H13NO2
Molecular Weight: 131.1729

Identification/Properties

Properties
BP:
255.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

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)-2-(Morpholin-3-yl)ethanol is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its chiral nature makes it particularly useful in asymmetric synthesis, allowing for the creation of enantiopure compounds with high stereoselectivity. In addition, (S)-2-(Morpholin-3-yl)ethanol can act as a ligand in metal-catalyzed reactions, enhancing catalytic efficiency and selectivity. Its ability to participate in a range of transformations, such as nucleophilic substitutions, reductive aminations, and ring-opening reactions, makes it an essential component in the toolbox of synthetic chemists. Whether utilized to introduce functionality, control stereochemistry, or facilitate complex transformations, (S)-2-(Morpholin-3-yl)ethanol plays a crucial role in advancing the field of chemical synthesis.