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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)-

1(2H)-Pyrimidineacetic acid, 3,4-dihydro-5-methyl-2,4-dioxo-

OC(=O)Cn1cc(C)c(=O)[nH]c1=O Request for Quotation
Chemical Name: 1(2H)-Pyrimidineacetic acid, 3,4-dihydro-5-methyl-2,4-dioxo-
CAS Number: 20924-05-4
Product Number: AG002K4A(AGN-PC-0JX24J)
Synonyms:
MDL No: MFCD00274250
Molecular Formula: C7H8N2O4
Molecular Weight: 184.1494

Identification/Properties

Properties
MP:
272-278 °C (dec.);(lit.);
BP:
424.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
184.151g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
184.048g/mol
Monoisotopic Mass:
184.048g/mol
Topological Polar Surface Area:
86.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
308
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-(5-Methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and reactive functional groups, this compound serves as a key intermediate in the synthesis of various complex organic molecules. Its ability to undergo diverse chemical transformations makes it valuable for the preparation of pharmaceuticals, agrochemicals, and advanced materials. In organic synthesis, 2-(5-Methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetic acid can participate in different reactions such as acylation, alkylation, and condensation, enabling the construction of intricate molecular frameworks. Additionally, its presence in the synthetic route can impart specific properties or functionalities to the final product, enhancing its utility in multiple industrial sectors.