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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)-

5-Pyrimidinecarboxylic acid, 1,2,3,4-tetrahydro-2-oxo-, ethyl ester

CCOC(=O)C1=CNC(=O)NC1 Request for Quotation
Chemical Name: 5-Pyrimidinecarboxylic acid, 1,2,3,4-tetrahydro-2-oxo-, ethyl ester
CAS Number: 33458-27-4
Product Number: AG00CL0U(AGN-PC-0NBJ0Z)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O3
Molecular Weight: 170.1659

Identification/Properties

Computed Properties
Molecular Weight:
170.168g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
170.069g/mol
Monoisotopic Mass:
170.069g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
235
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

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


Ethyl 2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key intermediate in the preparation of various heterocyclic compounds, providing a crucial building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Its unique structure and reactivity make $name$ a valuable tool in organic chemistry, allowing for the efficient introduction of functional groups and enabling the synthesis of complex molecules. By incorporating this compound into synthetic routes, chemists can streamline the production of target compounds and achieve high yields with excellent selectivity.In chemical synthesis, the application of Ethyl 2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate extends to the preparation of bioactive compounds, natural products, and advanced materials. Its versatile nature and compatibility with a wide range of reactions make it a valuable asset in the laboratory, facilitating the exploration of new synthetic pathways and the discovery of novel compounds with diverse applications.