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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-fluoro-4-(trifluoromethyl)phenyl]-

Fc1cc(ccc1N1CCNCC1)C(F)(F)F Request for Quotation
Chemical Name: Piperazine, 1-[2-fluoro-4-(trifluoromethyl)phenyl]-
CAS Number: 817170-70-0
Product Number: AG003DT4(AGN-PC-07YLOL)
Synonyms:
MDL No: MFCD11872764
Molecular Formula: C11H12F4N2
Molecular Weight: 248.2200

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
248.225g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
248.094g/mol
Monoisotopic Mass:
248.094g/mol
Topological Polar Surface Area:
15.3A^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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 1-(2-Fluoro-4-(trifluoromethyl)phenyl)piperazine, commonly referred to as $name$, is a versatile building block in chemical synthesis. Its strategic combination of a piperazine ring with a fluorinated phenyl group makes it a valuable intermediate in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, $name$ is used as a key starting material or intermediate for the development of diverse compounds due to its functional groups and reactivity. The piperazine ring confers biological activity in certain molecules, while the fluorinated phenyl group enhances the compound's lipophilicity and can influence interactions with biological targets. This unique combination makes $name$ particularly useful in medicinal chemistry for designing drug candidates with improved potency and pharmacokinetic properties.Additionally, the specific arrangement of functional groups in $name$ allows for further derivatization through various synthetic transformations. These modifications can tailor the compound's physicochemical properties and biological activity to meet specific requirements in drug discovery or material science applications. Overall, the utility of 1-(2-Fluoro-4-(trifluoromethyl)phenyl)piperazine in chemical synthesis lies in its versatility as a building block for designing advanced molecular structures with potential pharmacological or industrial significance.