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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)-

2,4(1H,3H)-Pyrimidinedione, 5,6-dimethyl-

Cc1[nH]c(=O)[nH]c(=O)c1C Request for Quotation
Chemical Name: 2,4(1H,3H)-Pyrimidinedione, 5,6-dimethyl-
CAS Number: 26305-13-5
Product Number: AG002SNK(AGN-PC-0JM1N7)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O2
Molecular Weight: 140.1399

Identification/Properties

Properties
MP:
297-300 °C (dec.);(lit.);
BP:
408.8°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.5065 (estimate)
Computed Properties
Molecular Weight:
140.142g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
140.059g/mol
Monoisotopic Mass:
140.059g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
230
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


5,6-Dimethyl-2,4(1H,3H)-pyrimidinedione is a versatile chemical compound commonly used in chemical synthesis. Its unique structure allows it to serve as a key building block in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. In organic synthesis, this compound can act as a precursor for the synthesis of pyrimidine derivatives with diverse biological activities. Additionally, 5,6-Dimethyl-2,4(1H,3H)-pyrimidinedione can be employed as a reagent in the formation of heterocyclic compounds and in the development of novel materials with specific properties. Its presence in the synthesis pathway can lead to the creation of compounds with improved pharmacological properties or enhanced performance in various applications.