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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)-

4-Pyrimidineacetic acid, 1,6-dihydro-2-methyl-6-oxo-, methyl ester

COC(=O)Cc1cc(=O)[nH]c(n1)C Request for Quotation
Chemical Name: 4-Pyrimidineacetic acid, 1,6-dihydro-2-methyl-6-oxo-, methyl ester
CAS Number: 93715-53-8
Product Number: AG00IHRJ(AGN-PC-0ONQ0C)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O3
Molecular Weight: 182.1766

Identification/Properties

Computed Properties
Molecular Weight:
182.179g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
182.069g/mol
Monoisotopic Mass:
182.069g/mol
Topological Polar Surface Area:
67.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
305
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


Methyl 2-(2-methyl-6-oxo-1,6-dihydropyrimidin-4-yl)acetate is a versatile compound commonly used in chemical synthesis. It serves as a valuable building block in organic chemistry reactions, particularly in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. This compound's unique structure allows for the modification of the dihydropyrimidine ring, enabling the synthesis of diverse molecular structures with various functionalities. Its presence in the reaction mixture can facilitate the formation of important intermediates or final products with enhanced biological or chemical properties. Additionally, the reactivity of the ester group in Methyl 2-(2-methyl-6-oxo-1,6-dihydropyrimidin-4-yl)acetate offers opportunities for derivatization, enabling the introduction of different substituents for further chemical transformations. In summary, the strategic use of Methyl 2-(2-methyl-6-oxo-1,6-dihydropyrimidin-4-yl)acetate in chemical synthesis opens up pathways for creating novel compounds with promising applications in various industries.