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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-Pyrimidinamine, N,4-dimethyl-

CNc1nccc(n1)C Request for Quotation
Chemical Name: 2-Pyrimidinamine, N,4-dimethyl-
CAS Number: 15231-63-7
Product Number: AG00B4ZJ(AGN-PC-0NJZ6I)
Synonyms:
MDL No:
Molecular Formula: C6H9N3
Molecular Weight: 123.1558

Identification/Properties

Computed Properties
Molecular Weight:
123.159g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
123.08g/mol
Monoisotopic Mass:
123.08g/mol
Topological Polar Surface Area:
37.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
84.4
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


N,4-Dimethylpyrimidin-2-amine, also known as DMPA, is a versatile compound commonly used in chemical synthesis for its valuable properties and functionality. This compound serves as a key building block in the creation of various pharmaceuticals and agrochemicals. In particular, N,4-Dimethylpyrimidin-2-amine is frequently employed in the synthesis of antiviral drugs, fungicides, and other biologically active compounds.Additionally, N,4-Dimethylpyrimidin-2-amine plays a crucial role as a precursor in the preparation of specialized reagents and catalysts used in organic chemistry reactions. Its unique structure and reactivity make it a preferred choice for introducing key functional groups or modifying specific molecular structures in the synthesis of complex organic molecules.Overall, N,4-Dimethylpyrimidin-2-amine is an essential component in the toolkit of chemists and researchers engaged in drug discovery, agrochemical development, and various branches of organic chemistry. Its application in chemical synthesis enables the efficient and precise construction of diverse compounds with significant biological or pharmaceutical implications.