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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)-

Acetamide, N-(1,2-dihydro-2-oxo-4-pyrimidinyl)-

CC(=O)Nc1ccnc(=O)[nH]1 Request for Quotation
Chemical Name: Acetamide, N-(1,2-dihydro-2-oxo-4-pyrimidinyl)-
CAS Number: 14631-20-0
Product Number: AG001DWJ(AGN-PC-0O39VO)
Synonyms:
MDL No: MFCD00134466
Molecular Formula: C6H7N3O2
Molecular Weight: 153.1387

Identification/Properties

Properties
MP:
>300 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
153.141g/mol
XLogP3:
-2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
153.054g/mol
Monoisotopic Mass:
153.054g/mol
Topological Polar Surface Area:
70.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
255
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


N-(2-Oxo-1,2-dihydropyrimidin-4-yl)acetamide is a versatile compound frequently employed in chemical synthesis due to its unique reactivity and structural properties. This molecule serves as a valuable building block for the construction of various heterocyclic compounds, pharmaceuticals, and agrochemicals. Its functional groups enable it to participate in multiple types of reactions, including condensation, alkylation, and substitution reactions. Moreover, the presence of the pyrimidine ring confers additional stability and rigidity to the synthesized products, enhancing their overall structural integrity. In addition to its utility in organic synthesis, N-(2-Oxo-1,2-dihydropyrimidin-4-yl)acetamide also exhibits promising biological activities, making it a key intermediate in the development of bioactive compounds with potential therapeutic applications.