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

CC(Cn1c(N)cc(=O)[nH]c1=O)C Request for Quotation
Chemical Name: 2,4(1H,3H)-Pyrimidinedione, 6-amino-1-(2-methylpropyl)-
CAS Number: 56075-75-3
Product Number: AG00DF3D(AGN-PC-0JX273)
Synonyms:
MDL No:
Molecular Formula: C8H13N3O2
Molecular Weight: 183.2077

Identification/Properties

Properties
MP:
258-261°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
183.211g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
183.101g/mol
Monoisotopic Mass:
183.101g/mol
Topological Polar Surface Area:
75.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
271
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-1-isobutylpyrimidine-2,4(1H,3H)-dione, also known as $name$, serves as a valuable building block in chemical synthesis processes. Due to its unique structure and reactivity, this compound is commonly employed in the development of various organic compounds and pharmaceutical intermediates. Its versatility allows for the creation of complex molecules through key reactions such as acylation, alkylation, and condensation. $name$ plays a crucial role in the synthesis of diverse materials, enabling chemists to access novel compounds for research and development purposes.