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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-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]aniline

CN1CCN(CC1)C1CCN(CC1)c1ccc(cc1)N Request for Quotation
Chemical Name: 4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]aniline
CAS Number: 959795-70-1
Product Number: AG005WD4(AGN-PC-0C4UJH)
Synonyms:
MDL No:
Molecular Formula: C16H26N4
Molecular Weight: 274.4044

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
274.412g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
274.216g/mol
Monoisotopic Mass:
274.216g/mol
Topological Polar Surface Area:
35.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
285
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


4-(4-(4-Methylpiperazin-1-yl)piperidin-1-yl)aniline is a versatile compound frequently utilized in chemical synthesis as a key building block for the development of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structural properties make it an essential intermediate in the creation of complex organic molecules with diverse applications.In chemical synthesis, this compound serves as a valuable precursor for the preparation of novel drug candidates due to its ability to introduce specific functional groups and molecular motifs that are crucial for enhancing biological activity and pharmacokinetic profiles. By incorporating 4-(4-(4-Methylpiperazin-1-yl)piperidin-1-yl)aniline into the molecular structure of target compounds, chemists can modulate their physicochemical properties, optimize their potency, and improve their overall therapeutic efficacy.Furthermore, the versatility of 4-(4-(4-Methylpiperazin-1-yl)piperidin-1-yl)aniline extends beyond medicinal chemistry, finding applications in the synthesis of specialty chemicals, polymers, and materials with tailored functionalities. Its strategic placement within a synthetic pathway enables chemists to access novel molecular architectures and design compounds with specific performance characteristics for various industrial sectors.Overall, the strategic incorporation of 4-(4-(4-Methylpiperazin-1-yl)piperidin-1-yl)aniline in chemical synthesis empowers researchers to explore new avenues in drug discovery, material science, and chemical innovation, paving the way for the development of cutting-edge products with significant societal impact.