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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)-

1-Piperazineethanol, 4-[(4-fluorophenyl)methyl]-

OCCN1CCN(CC1)Cc1ccc(cc1)F Request for Quotation
Chemical Name: 1-Piperazineethanol, 4-[(4-fluorophenyl)methyl]-
CAS Number: 174561-11-6
Product Number: AG001ZS8(AGN-PC-0JV1D6)
Synonyms:
MDL No:
Molecular Formula: C13H19FN2O
Molecular Weight: 238.3012

Identification/Properties

Properties
MP:
55℃
Form:
Solid
Computed Properties
Molecular Weight:
238.306g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
238.148g/mol
Monoisotopic Mass:
238.148g/mol
Topological Polar Surface Area:
26.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
212
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


2-(4-(4-Fluorobenzyl)piperazin-1-yl)ethanol, also known as $name$, is a crucial compound in chemical synthesis due to its versatile applications. In organic synthesis, this compound is frequently used as a key intermediate in the preparation of various pharmaceuticals and fine chemicals. Its unique chemical structure makes it an essential building block in the synthesis of diverse heterocyclic compounds and bioactive molecules.One of the prominent applications of 2-(4-(4-Fluorobenzyl)piperazin-1-yl)ethanol is its role as a precursor in the synthesis of functionalized piperazine derivatives. These derivatives have demonstrated promising pharmacological activities, including anti-cancer, antibacterial, and antipsychotic properties. The presence of the piperazine moiety in the molecular structure imparts specific biological functions to the synthesized compounds, making them valuable in drug discovery and development.Furthermore, 2-(4-(4-Fluorobenzyl)piperazin-1-yl)ethanol serves as a valuable starting material in the preparation of ligands for metal-catalyzed reactions and complex organic transformations. Its ability to undergo selective functionalization at the piperazine nitrogen and the benzyl ring enables the synthesis of tailored ligands with precise stereochemical control, making it a preferred choice in asymmetric catalysis and coordination chemistry.Overall, the application of 2-(4-(4-Fluorobenzyl)piperazin-1-yl)ethanol in chemical synthesis showcases its significance as a versatile and indispensable compound in the development of diverse organic molecules with valuable functional properties. This compound's strategic position as an intermediate allows for the efficient synthesis of complex molecules with specific biological, catalytic, and pharmaceutical applications.