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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)-

2H-Imidazol-2-one, 1-(4-chlorophenyl)-1,5-dihydro-4-(4-morpholinyl)-

O=C1N=C(CN1c1ccc(cc1)Cl)N1CCOCC1 Request for Quotation
Chemical Name: 2H-Imidazol-2-one, 1-(4-chlorophenyl)-1,5-dihydro-4-(4-morpholinyl)-
CAS Number: 188116-07-6
Product Number: AG002GP9(AGN-PC-0KP02Q)
Synonyms:
MDL No:
Molecular Formula: C13H14ClN3O2
Molecular Weight: 279.7222

Identification/Properties

Properties
MP:
264℃ (ethanol )
BP:
421.8±55.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
279.724g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
279.077g/mol
Monoisotopic Mass:
279.077g/mol
Topological Polar Surface Area:
45.1A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
374
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one, commonly known as $name$, is a versatile compound used in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the creation of various bioactive molecules and pharmaceuticals due to its structural features and functional groups.In chemical synthesis, $name$ can act as a versatile intermediate for the creation of new compounds through various synthetic routes. Its imidazolone core provides a valuable starting point for the modification and functionalization of the molecule, allowing chemists to customize its structure for specific applications. The presence of the chlorophenyl and morpholinyl groups further enhances the reactivity and potential interactions of $name$ in synthetic reactions.One common application of 1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one in chemical synthesis is in the development of novel pharmaceutical agents. By introducing specific substituents or functional groups onto the imidazolone scaffold, chemists can create drug candidates with potential therapeutic properties. The incorporation of the morpholinyl group can also contribute to the compound's pharmacokinetic profile, impacting factors such as solubility and bioavailability.Furthermore, the reactivity of $name$ makes it a valuable tool for medicinal chemists seeking to optimize the biological activity and properties of lead compounds. By utilizing this versatile building block in strategic chemical transformations, researchers can explore new structures and improve the potency, selectivity, and safety profiles of drug candidates.Overall, 1-(4-chlorophenyl)-4-morpholin-4-yl-5H-imidazol-2-one plays a crucial role in chemical synthesis by offering a platform for the creation of diverse molecules with applications in drug discovery, materials science, and other fields requiring tailored compounds with specific functionalities.