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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)-

1,3-dimethyl-5H-pyrrolo[3,2-d]pyrimidine-2,4-dione

Cn1c(=O)n(C)c2c(c1=O)[nH]cc2 Request for Quotation
Chemical Name: 1,3-dimethyl-5H-pyrrolo[3,2-d]pyrimidine-2,4-dione
CAS Number: 46155-89-9
Product Number: AG00DKE7(AGN-PC-0JN14F)
Synonyms:
MDL No:
Molecular Formula: C8H9N3O2
Molecular Weight: 179.1760

Identification/Properties

Computed Properties
Molecular Weight:
179.179g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
179.069g/mol
Monoisotopic Mass:
179.069g/mol
Topological Polar Surface Area:
56.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
266
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


1,3-Dimethyl-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione is a versatile molecule commonly utilized in chemical synthesis due to its unique structural properties. In organic chemistry, it serves as a key intermediate in the preparation of various heterocyclic compounds with diverse applications. The presence of nitrogen and oxygen atoms in its molecular framework makes it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and materials with specific properties. Its condensed heterocyclic structure allows for the introduction of functional groups at multiple positions, enabling the generation of complex molecular architectures. Additionally, the electron-rich nature of the pyrrolopyrimidine core facilitates reactions with electrophiles, nucleophiles, and radical species, broadening its synthetic utility in diverse chemical transformations. As a result, 1,3-Dimethyl-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione plays a crucial role in the synthesis of novel compounds with potential applications in medicinal chemistry, material science, and other fields.