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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)-

Piperidine, 4-[4-(trifluoromethoxy)phenoxy]-

FC(Oc1ccc(cc1)OC1CCNCC1)(F)F Request for Quotation
Chemical Name: Piperidine, 4-[4-(trifluoromethoxy)phenoxy]-
CAS Number: 287952-67-4
Product Number: AG002WIJ(AGN-PC-00TXVQ)
Synonyms:
MDL No:
Molecular Formula: C12H14F3NO2
Molecular Weight: 261.2403

Identification/Properties

Properties
MP:
71-73°C
BP:
295.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
261.244g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
261.098g/mol
Monoisotopic Mass:
261.098g/mol
Topological Polar Surface Area:
30.5A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
246
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(4-Trifluoromethoxyphenoxy)piperidine is a versatile compound used in chemical synthesis for the development of pharmaceuticals, agrochemicals, and specialty materials. This unique molecule serves as a key building block in the creation of advanced organic compounds due to its distinct chemical properties and reactivity.In chemical synthesis, 4-(4-Trifluoromethoxyphenoxy)piperidine can be utilized as a precursor for the synthesis of diverse heterocyclic compounds, such as potent drug candidates and functional materials. Its piperidine ring confers structural stability and biological activity to the synthesized molecules, making it an essential ingredient in the production of various organic compounds.Furthermore, the trifluoromethoxyphenoxy moiety attached to the piperidine ring enhances the overall physicochemical properties of the synthesized compounds, such as increased lipophilicity and metabolic stability. This modification can lead to improved bioavailability and pharmacokinetic profiles of the final products, making them more effective for their intended applications.Overall, the application of 4-(4-Trifluoromethoxyphenoxy)piperidine in chemical synthesis allows for the efficient and strategic construction of complex molecules with diverse functionalities, paving the way for the development of innovative and valuable compounds for various industries.