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  2. 2,4(1H,3H)-Pyrimidinedione, 6-amino-3-methyl-1-(2-methylpropyl)-

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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-amino-3-methyl-1-(2-methylpropyl)-

CC(Cn1c(N)cc(=O)n(c1=O)C)C Request for Quotation
Chemical Name: 2,4(1H,3H)-Pyrimidinedione, 6-amino-3-methyl-1-(2-methylpropyl)-
CAS Number: 58481-39-3
Product Number: AG00EEZQ(AGN-PC-0JNPTJ)
Synonyms:
MDL No:
Molecular Formula: C9H15N3O2
Molecular Weight: 197.2343

Identification/Properties

Computed Properties
Molecular Weight:
197.238g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
197.116g/mol
Monoisotopic Mass:
197.116g/mol
Topological Polar Surface Area:
66.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
296
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


6-Amino-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione, also known as $name$, serves a vital role in chemical synthesis as a versatile building block. Its unique chemical structure makes it a valuable intermediate in the creation of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, $name$ can be employed as a key starting material for the production of heterocyclic compounds. Its amino and carbonyl functional groups make it an essential component in the formation of more complex molecules through reactions such as acylation, alkylation, and cyclization. The presence of the isobutyl and methyl groups enhances the reactivity and selectivity of these reactions, allowing for the controlled synthesis of desired products.Additionally, the pyrimidine ring system in $name$ confers specific properties to the resulting compounds, making them valuable in medicinal chemistry and material science. By strategically incorporating $name$ into synthesis pathways, chemists can access a diverse array of compounds with potential applications in drug discovery, crop protection, and the development of novel materials.Overall, the strategic utilization of 6-Amino-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione in chemical synthesis enables the efficient construction of complex molecules with tailored properties, driving innovation in various industries.