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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)-

Ethanone, 1-[4-[4-amino-2-(trifluoromethyl)phenyl]-1-piperazinyl]-

Nc1ccc(c(c1)C(F)(F)F)N1CCN(CC1)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-[4-[4-amino-2-(trifluoromethyl)phenyl]-1-piperazinyl]-
CAS Number: 914348-88-2
Product Number: AG00GUMY(AGN-PC-05W4E3)
Synonyms:
MDL No:
Molecular Formula: C13H16F3N3O
Molecular Weight: 287.2808496

Identification/Properties

Computed Properties
Molecular Weight:
287.286g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
287.125g/mol
Monoisotopic Mass:
287.125g/mol
Topological Polar Surface Area:
49.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
353
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


Ethanone, 1-[4-[4-amino-2-(trifluoromethyl)phenyl]-1-piperazinyl]- is a versatile chemical compound commonly utilized in chemical synthesis for its unique properties and diverse applications. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, Ethanone plays a crucial role as a key intermediate in the development of novel compounds with potential therapeutic benefits. Its structural features allow for efficient and precise modifications, making it a preferred choice for designing molecules with specific biological activities.Additionally, Ethanone's functional groups enable it to participate in a wide range of synthetic reactions, such as nucleophilic addition, substitution, and condensation, facilitating the synthesis of complex organic molecules. This compound's compatibility with different reaction conditions and its stability make it an essential tool for chemists in the creation of diverse chemical compounds.Overall, the application of Ethanone, 1-[4-[4-amino-2-(trifluoromethyl)phenyl]-1-piperazinyl]- in chemical synthesis showcases its significance in the development of new materials and compounds with potential industrial and medicinal applications.