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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)-

4-piperazin-1-ylpyrimidine;dihydrochloride

N1CCN(CC1)c1ccncn1.Cl.Cl Request for Quotation
Chemical Name: 4-piperazin-1-ylpyrimidine;dihydrochloride
CAS Number: 634468-72-7
Product Number: AG00EICU(AGN-PC-0H0YHY)
Synonyms:
MDL No:
Molecular Formula: C8H14Cl2N4
Molecular Weight: 237.1296

Identification/Properties

Computed Properties
Molecular Weight:
237.128g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
236.06g/mol
Monoisotopic Mass:
236.06g/mol
Topological Polar Surface Area:
41A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
133
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Piperazin-1-yl)pyrimidine dihydrochloride is a versatile compound commonly used in chemical synthesis as a building block for the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and properties make it a valuable intermediate in the production of diverse compounds with biological activity.In organic synthesis, 4-(Piperazin-1-yl)pyrimidine dihydrochloride serves as a key starting material for the preparation of complex molecules due to its functional groups that can participate in a variety of chemical reactions. It can undergo various transformations such as substitution, formylation, and alkylation to introduce different substituents onto the pyrimidine ring, allowing for the generation of structurally diverse compounds.Furthermore, the presence of the piperazine moiety in 4-(Piperazin-1-yl)pyrimidine dihydrochloride provides the opportunity for interactions with biological targets, making it particularly valuable in medicinal chemistry. This compound can be further modified to enhance its pharmacological properties, leading to the discovery of novel drugs and therapeutic agents.Overall, the application of 4-(Piperazin-1-yl)pyrimidine dihydrochloride in chemical synthesis contributes to the development of new molecules with potential biological activities, making it an important tool in drug discovery and other areas of applied chemistry.