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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)-

Piperazine, 1-(2,4-dimethylphenyl)-

Cc1ccc(c(c1)C)N1CCNCC1 Request for Quotation
Chemical Name: Piperazine, 1-(2,4-dimethylphenyl)-
CAS Number: 1013-76-9
Product Number: AG00046T(AGN-PC-0JL9RL)
Synonyms:
MDL No:
Molecular Formula: C12H18N2
Molecular Weight: 190.2847

Identification/Properties

Properties
BP:
153°C/10mmHg(lit.)
Storage:
2-8℃;
Form:
Liquid
Refractive Index:
1.553-1.555
Computed Properties
Molecular Weight:
190.29g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
190.147g/mol
Monoisotopic Mass:
190.147g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
175
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


1-(2,4-Dimethylphenyl)piperazine, commonly known as $name$, is a versatile compound with significant relevance in chemical synthesis. This unique molecule serves as a vital building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its distinct chemical structure, comprising a piperazine ring and a 2,4-dimethylphenyl moiety, imparts specific reactivity and functionality that make it a key intermediate in the synthesis of complex organic compounds. The presence of the piperazine ring offers opportunities for potential interactions with biological targets, highlighting its importance in drug discovery and development. Additionally, the 2,4-dimethylphenyl group can provide steric hindrance and electronic effects, influencing the overall properties and activity of the final products. In chemical synthesis, $name$ can be employed as a precursor for the preparation of diverse molecules, including antipsychotics, antidepressants, and anticancer agents. Its strategic incorporation into molecular frameworks allows for the modulation of pharmacological properties, enhancing efficacy and reducing side effects. Overall, the application of 1-(2,4-Dimethylphenyl)piperazine in chemical synthesis underscores its pivotal role in advancing the field of medicinal and organic chemistry.