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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, 6-phenyl-

O=c1[nH]c(=O)[nH]c(c1)c1ccccc1 Request for Quotation
Chemical Name: 2,4(1H,3H)-Pyrimidinedione, 6-phenyl-
CAS Number: 13345-09-0
Product Number: AG007NFB(AGN-PC-00H4ID)
Synonyms:
MDL No:
Molecular Formula: C10H8N2O2
Molecular Weight: 188.1827

Identification/Properties

Computed Properties
Molecular Weight:
188.186g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
188.059g/mol
Monoisotopic Mass:
188.059g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
291
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


6-Phenylpyrimidine-2,4(1H,3H)-dione, a versatile building block in chemical synthesis, is widely utilized in the production of various pharmaceuticals, agrochemicals, and materials. This compound serves as a key intermediate in the synthesis of several biologically active compounds, including anticancer and antiviral drugs. Its unique molecular structure and reactivity make it an essential component in the creation of complex organic molecules. Additionally, 6-Phenylpyrimidine-2,4(1H,3H)-dione plays a crucial role in the development of novel chemical entities with potential pharmacological applications. Its efficient incorporation in multistep synthetic pathways highlights its significance in the field of medicinal chemistry and drug discovery.