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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)-

3-Pyridinecarboxylicacid, 6-(4-methyl-1-piperazinyl)-

CN1CCN(CC1)c1ccc(cn1)C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylicacid, 6-(4-methyl-1-piperazinyl)-
CAS Number: 132521-70-1
Product Number: AG0010RT(AGN-PC-00384E)
Synonyms:
MDL No:
Molecular Formula: C11H15N3O2
Molecular Weight: 221.2557

Identification/Properties

Computed Properties
Molecular Weight:
221.26g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
221.116g/mol
Monoisotopic Mass:
221.116g/mol
Topological Polar Surface Area:
56.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
252
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


6-(4-Methylpiperazin-1-yl)nicotinic acid, often referred to as $name$, plays a crucial role in chemical synthesis due to its unique properties and versatile applications. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. With its strategic placement of a methylpiperazine and nicotinic acid moiety, $name$ offers a strong foundation for the development of new drug candidates and bioactive molecules. In organic synthesis, it serves as a valuable intermediate for the construction of complex chemical structures with enhanced biological activities. The incorporation of 6-(4-Methylpiperazin-1-yl)nicotinic acid into diverse molecular frameworks enables the synthesis of potent pharmaceuticals with targeted pharmacological properties. Furthermore, its compatibility with different reaction conditions and functional groups makes it a valuable tool for the design and synthesis of innovative compounds in medicinal chemistry and material science.