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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-propyl-

Cn1c(=O)n(CCC)c(cc1=O)N Request for Quotation
Chemical Name: 2,4(1H,3H)-Pyrimidinedione, 6-amino-3-methyl-1-propyl-
CAS Number: 53681-48-4
Product Number: AG00DH3H(AGN-PC-0JLEF2)
Synonyms:
MDL No:
Molecular Formula: C8H13N3O2
Molecular Weight: 183.2077

Identification/Properties

Computed Properties
Molecular Weight:
183.211g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
183.101g/mol
Monoisotopic Mass:
183.101g/mol
Topological Polar Surface Area:
66.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
273
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-Amino-3-methyl-1-propylpyrimidine-2,4(1H,3H)-dione, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it an essential building block in organic chemistry.In chemical synthesis, $name$ serves as a key intermediate for the preparation of a variety of pharmaceuticals, agrochemicals, and other fine chemicals. Its amino and carbonyl functional groups enable it to participate in numerous reactions, such as nucleophilic substitution, condensation, and cyclization reactions.One common application of 6-Amino-3-methyl-1-propylpyrimidine-2,4(1H,3H)-dione is in the synthesis of heterocyclic compounds, which are prevalent in medicinal chemistry due to their diverse biological activities. By incorporating $name$ into these synthetic routes, chemists can access novel compounds with potential therapeutic properties.Additionally, 6-Amino-3-methyl-1-propylpyrimidine-2,4(1H,3H)-dione can be utilized in the development of new materials, such as polymers and dyes, further highlighting its significance in the field of chemical synthesis. Its versatility and reactivity make it a valuable tool for chemists seeking to create complex molecules with specific functionalities.