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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-5-amine

CN1CCN(CC1)c1ncc(cn1)N Request for Quotation
Chemical Name: 2-(4-methylpiperazin-1-yl)pyrimidin-5-amine
CAS Number: 943757-74-2
Product Number: AG00II3S(AGN-PC-0BIG38)
Synonyms:
MDL No:
Molecular Formula: C9H15N5
Molecular Weight: 193.2489

Identification/Properties

Computed Properties
Molecular Weight:
193.254g/mol
XLogP3:
-0.2
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:
170
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-(4-Methylpiperazin-1-yl)pyrimidin-5-amine is a versatile intermediate that finds significant application in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, the presence of the piperazine moiety enables the compound to effectively participate in nucleophilic substitution reactions, allowing for the introduction of diverse functional groups. Moreover, the pyrimidine ring provides structural diversity and imparts specific properties to the final products. Due to its strategic positioning within the molecule, 2-(4-Methylpiperazin-1-yl)pyrimidin-5-amine plays a crucial role in the preparation of innovative compounds with potential biological activities or other desired characteristics. Its unique combination of functional groups makes it a valuable tool for synthetic chemists, enabling the creation of complex molecules in a controlled and efficient manner.