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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)-

2-Morpholinone, 5-phenyl-, (5S)-

O=C1OC[C@@H](NC1)c1ccccc1 Request for Quotation
Chemical Name: 2-Morpholinone, 5-phenyl-, (5S)-
CAS Number: 144896-92-4
Product Number: AG001KB5(AGN-PC-0O2Z6E)
Synonyms:
MDL No:
Molecular Formula: C10H11NO2
Molecular Weight: 177.1998

Identification/Properties

Computed Properties
Molecular Weight:
177.203g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
177.079g/mol
Monoisotopic Mass:
177.079g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
187
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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


(S)-5-Phenylmorpholin-2-one, also known as (S)-2-oxo-5-phenylmorpholine, is a versatile chemical compound widely used in chemical synthesis for various applications. It serves as a key building block for the preparation of diverse organic compounds due to its unique structure and reactivity.In chemical synthesis, (S)-5-Phenylmorpholin-2-one is frequently employed as a chiral auxiliary to induce stereochemical control in asymmetric transformations. Its presence in a reaction can influence the stereochemistry of the products formed, allowing for the selective synthesis of enantiomerically pure compounds. This is particularly useful in the pharmaceutical industry where enantiopure compounds are essential for drug development.Additionally, (S)-5-Phenylmorpholin-2-one can function as a versatile intermediate in the synthesis of complex molecules such as natural products, pharmaceuticals, and agrochemicals. Its morpholine ring and phenyl group provide versatility in forming various chemical bonds and functional groups, making it a valuable tool for organic chemists.Furthermore, the (S)-configuration of this compound is crucial in certain reactions where stereochemistry plays a significant role in the outcome. By utilizing (S)-5-Phenylmorpholin-2-one in these reactions, chemists can achieve high levels of stereocontrol, ultimately leading to the targeted synthesis of specific enantiomers.Overall, (S)-5-Phenylmorpholin-2-one plays a pivotal role in chemical synthesis by enabling precise stereochemical control and serving as a versatile intermediate for the preparation of diverse organic compounds. Its significance in asymmetric synthesis and the production of enantiopure compounds make it a valuable tool for synthetic chemists across various industries.