5-propan-2-ylmorpholin-3-one|127958-60-5,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

5-propan-2-ylmorpholin-3-one

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Chemical Name:	5-propan-2-ylmorpholin-3-one
CAS Number:	127958-60-5
Product Number:	AG000XLZ(AGN-PC-02LWV7)
Synonyms:
MDL No:
Molecular Formula:	C7H13NO2
Molecular Weight:	143.1836

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Identification/Properties

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NMR Spectrum

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Chemical Structure

(S)-5-Isopropylmorpholin-3-one is a versatile compound commonly utilized in chemical synthesis due to its unique structural properties. This molecule is highly valued for its chirality and functional groups, which make it a valuable building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. In organic synthesis, (S)-5-Isopropylmorpholin-3-one can serve as a key intermediate in the creation of complex molecules through processes such as asymmetric synthesis, chiral resolution, and stereocontrolled reactions. Its presence can significantly influence the stereochemistry and overall molecular structure of the final product, making it a crucial tool for chemists seeking to produce enantiomerically pure compounds with specific desired properties.