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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-[4-(trifluoromethyl)phenyl]piperidin-4-ol

OC1CCN(CC1)c1ccc(cc1)C(F)(F)F Request for Quotation
Chemical Name: 1-[4-(trifluoromethyl)phenyl]piperidin-4-ol
CAS Number: 681508-70-3
Product Number: AG00FAYO(AGN-PC-03KAYT)
Synonyms:
MDL No:
Molecular Formula: C12H14F3NO
Molecular Weight: 245.2409

Identification/Properties

Computed Properties
Molecular Weight:
245.245g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
245.103g/mol
Monoisotopic Mass:
245.103g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
241
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


1-(4-Trifluoromethylphenyl)piperidin-4-ol is a versatile compound commonly used in chemical synthesis due to its unique chemical properties. This compound is known for its ability to serve as a valuable building block in the creation of various organic molecules. Its structural composition allows it to participate in a range of chemical reactions, making it a valuable tool for synthetic chemists.In chemical synthesis, 1-(4-Trifluoromethylphenyl)piperidin-4-ol can be utilized as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and materials science applications. Its piperidine ring serves as a scaffold for further functionalization, allowing for the incorporation of diverse chemical functionalities. The trifluoromethyl group provides increased hydrophobicity and electron density, offering unique reactivity in organic transformations.Moreover, the hydroxyl group in 1-(4-Trifluoromethylphenyl)piperidin-4-ol enables the introduction of additional functionalities through selective derivatization, further expanding its utility in chemical synthesis. Whether employed in the construction of complex natural products or the development of novel drug candidates, this compound plays a critical role in advancing synthetic chemistry research and applications.