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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)-

Quinoline, 4-methyl-2-(1-piperazinyl)-

Cc1cc(nc2c1cccc2)N1CCNCC1 Request for Quotation
Chemical Name: Quinoline, 4-methyl-2-(1-piperazinyl)-
CAS Number: 50693-78-2
Product Number: AG003LPW(AGN-PC-0JTJTU)
Synonyms:
MDL No:
Molecular Formula: C14H17N3
Molecular Weight: 227.3049

Identification/Properties

Properties
BP:
432°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
227.311g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
227.142g/mol
Monoisotopic Mass:
227.142g/mol
Topological Polar Surface Area:
28.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
250
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methyl-2-(piperazin-1-yl)quinoline is a versatile chemical compound commonly used in chemical synthesis as a key intermediate in the production of pharmaceuticals and agrochemicals. With its unique molecular structure, this compound plays a crucial role in the development of various organic compounds due to its reactivity and functional groups. Specifically, 4-Methyl-2-(piperazin-1-yl)quinoline is employed in the synthesis of novel drugs and biologically active molecules by serving as a building block or precursor in the creation of complex organic structures. Its presence in chemical reactions allows for the formation of diverse molecular architectures that exhibit desirable pharmacological properties or agricultural effects. In chemical synthesis, the strategic incorporation of 4-Methyl-2-(piperazin-1-yl)quinoline enables the modification and enhancement of molecules, leading to the development of new compounds with potential therapeutic benefits or agricultural applications.