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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-(trifluoromethyl)benzoyl]-

O=C(c1ccccc1C(F)(F)F)N1CCNCC1 Request for Quotation
Chemical Name: Piperazine, 1-[2-(trifluoromethyl)benzoyl]-
CAS Number: 179534-78-2
Product Number: AG002728(AGN-PC-0151GP)
Synonyms:
MDL No: MFCD08442668
Molecular Formula: C12H13F3N2O
Molecular Weight: 258.2396

Identification/Properties

Computed Properties
Molecular Weight:
258.244g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
258.098g/mol
Monoisotopic Mass:
258.098g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
300
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


Piperazin-1-yl(2-(trifluoromethyl)phenyl)methanone is a versatile compound widely utilized in chemical synthesis due to its unique properties. This compound serves as a valuable building block in the pharmaceutical industry, particularly in the development of novel medications. Its strategic incorporation in drug design can enhance the biological activity and pharmacokinetic profiles of pharmaceutical agents. Furthermore, Piperazin-1-yl(2-(trifluoromethyl)phenyl)methanone exhibits reactivity in synthetic organic chemistry, facilitating the preparation of diverse molecular structures with potential therapeutic applications. Its structural features allow for functional group transformations, enabling the efficient synthesis of complex molecules. In summary, the application of Piperazin-1-yl(2-(trifluoromethyl)phenyl)methanone in chemical synthesis contributes significantly to the advancement of pharmaceutical research and the creation of innovative drug candidates.