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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-Pyrimidinecarboxylic acid, methyl ester

COC(=O)c1ccncn1 Request for Quotation
Chemical Name: 4-Pyrimidinecarboxylic acid, methyl ester
CAS Number: 2450-08-0
Product Number: AG002OD3(AGN-PC-0JNS16)
Synonyms:
MDL No:
Molecular Formula: C6H6N2O2
Molecular Weight: 138.1240

Identification/Properties

Computed Properties
Molecular Weight:
138.126g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
138.043g/mol
Monoisotopic Mass:
138.043g/mol
Topological Polar Surface Area:
52.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
127
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


Methyl pyrimidine-4-carboxylate is a versatile compound widely used in chemical synthesis as a key building block for the construction of various organic molecules. Its unique structure and reactivity make it an essential intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. By undergoing various transformations and functionalization reactions, Methyl pyrimidine-4-carboxylate can be tailored to introduce specific functionalities or structural motifs into target molecules. This compound's application in the synthesis of biologically active compounds highlights its importance in drug discovery and development. Additionally, its compatibility with a range of synthetic methodologies and its relatively straightforward preparation make Methyl pyrimidine-4-carboxylate a valuable tool for organic chemists seeking to access diverse chemical space and create novel molecules with potential pharmacological or industrial applications.