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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)-

Pyrimidinetriamine

Nc1ncc(c(n1)N)N Request for Quotation
Chemical Name: Pyrimidinetriamine
CAS Number: 3546-50-7
Product Number: AG00I71F(AGN-PC-0JMW74)
Synonyms:
MDL No:
Molecular Formula: C4H7N5
Molecular Weight: 125.1319

Identification/Properties

Computed Properties
Molecular Weight:
125.135g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
125.07g/mol
Monoisotopic Mass:
125.07g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
95
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


Pyrimidine-2,4,5-triamine, also known as isocytosine, is a versatile compound widely used in chemical synthesis. With its unique structure and reactive properties, this compound serves as a key building block in the creation of various organic molecules. In chemical synthesis, Pyrimidine-2,4,5-triamine plays a crucial role as a precursor for the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its ability to participate in diverse chemical reactions makes it a valuable component in the development of novel compounds with potential applications in various industries. By harnessing the chemical reactivity of Pyrimidine-2,4,5-triamine, chemists can embark on the creation of intricate molecular structures and explore new avenues for innovation in the field of organic chemistry.