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

CN1CCN(CC1)c1nccc(n1)N Request for Quotation
Chemical Name: 2-(4-methylpiperazin-1-yl)pyrimidin-4-amine
CAS Number: 57005-71-7
Product Number: AG00EK1Z(AGN-PC-07HAWE)
Synonyms:
MDL No:
Molecular Formula: C9H15N5
Molecular Weight: 193.2489

Identification/Properties

Properties
BP:
386.3±52.0°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
193.254g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
193.133g/mol
Monoisotopic Mass:
193.133g/mol
Topological Polar Surface Area:
58.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
178
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Methylpiperazin-1-yl)pyrimidin-4-amine is a versatile compound widely utilized in chemical synthesis as a key intermediate for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as a crucial building block in the synthesis of novel drug candidates, particularly in the field of medicinal chemistry and drug discovery. Its unique structure and reactivity enable chemists to introduce specific functional groups and modify the molecule to tailor its properties for specific applications. Additionally, 2-(4-Methylpiperazin-1-yl)pyrimidin-4-amine plays a significant role in the development of new materials and bioactive compounds, showcasing its importance in advancing the field of organic chemistry.