4-(4-methylpiperazin-1-yl)pyrimidin-2-amine|856973-81-4,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

4-(4-methylpiperazin-1-yl)pyrimidin-2-amine

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Chemical Name:	4-(4-methylpiperazin-1-yl)pyrimidin-2-amine
CAS Number:	856973-81-4
Product Number:	AG00GM5Z(AGN-PC-04WVDN)
Synonyms:
MDL No:
Molecular Formula:	C9H15N5
Molecular Weight:	193.2489

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Chemical Structure

4-(4-Methylpiperazin-1-yl)pyrimidin-2-amine, also known as $name$, is a versatile compound widely used in chemical synthesis. This unique molecule serves as a key building block in the creation of pharmaceuticals, agrochemicals, and materials due to its valuable structural features. Chemists utilize $name$ in the synthesis of novel drug candidates, where its functional groups can be strategically modified to enhance biological activity and target specificity. In addition, $name$ plays a crucial role in the development of new molecular tools and probes for biochemical research, enabling scientists to investigate complex biological processes. Its compatibility with various synthetic methods and diverse range of applications make $name$ a valuable asset in the realm of organic chemistry.