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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)-

4,6-Pyrimidinedicarboxylic acid, dimethyl ester

COC(=O)c1ncnc(c1)C(=O)OC Request for Quotation
Chemical Name: 4,6-Pyrimidinedicarboxylic acid, dimethyl ester
CAS Number: 6345-43-3
Product Number: AG00EE6M(AGN-PC-0JOEQJ)
Synonyms:
MDL No:
Molecular Formula: C8H8N2O4
Molecular Weight: 196.1601

Identification/Properties

Properties
MP:
78-79 °C
BP:
305.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
196.162g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
196.048g/mol
Monoisotopic Mass:
196.048g/mol
Topological Polar Surface Area:
78.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
209
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


Dimethyl pyrimidine-4,6-dicarboxylate, also known as DMPDC, serves as a valuable intermediate in chemical synthesis processes. This compound is widely utilized in organic chemistry for its ability to act as a versatile building block in the creation of various complex molecules. Its unique chemical structure enables it to participate in a range of reactions, making it a valuable tool for synthesizing novel compounds with diverse functionalities.DMPDC is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its presence in the reaction mixture can facilitate the formation of heterocyclic compounds, which are prevalent in many biologically active molecules. By incorporating DMPDC into the synthesis pathway, chemists can efficiently construct intricate molecular frameworks that are essential for drug discovery and materials science.Furthermore, DMPDC's reactivity allows for the introduction of different functional groups, enabling the modification of its chemical properties to tailor the desired characteristics of the final product. This flexibility in chemical manipulation makes DMPDC a valuable component in the toolbox of synthetic chemists seeking to access a diverse array of molecular structures for various applications.In summary, the application of Dimethyl pyrimidine-4,6-dicarboxylate in chemical synthesis extends beyond its role as a simple intermediate; it offers a versatile platform for the construction of complex molecules with tailored functionalities, making it an indispensable resource for advancing the field of organic chemistry.