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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-acetyl-4-(4-aminophenyl)-

CC(=O)N1CCN(CC1)c1ccc(cc1)N Request for Quotation
Chemical Name: Piperazine, 1-acetyl-4-(4-aminophenyl)-
CAS Number: 92394-00-8
Product Number: AG0066MX(AGN-PC-0JVOA9)
Synonyms:
MDL No: MFCD01365904
Molecular Formula: C12H17N3O
Molecular Weight: 219.2829

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
219.288g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
219.137g/mol
Monoisotopic Mass:
219.137g/mol
Topological Polar Surface Area:
49.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
241
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-Acetyl-1-piperazinyl)aniline is a versatile compound that finds wide application in chemical synthesis. Its unique structure enables it to be utilized as a key building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Specifically, this compound can serve as a valuable intermediate in the synthesis of novel drugs, targeting a range of therapeutic areas such as anti-cancer, anti-inflammatory, and antimicrobial agents. Additionally, its functional groups make it a valuable precursor in the development of advanced materials and organic coatings. In the realm of chemical research, 4-(4-Acetyl-1-piperazinyl)aniline offers a promising platform for the creation of diverse molecular structures with potential biological activities.