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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-(2-fluoroethyl)piperidin-4-amine

FCCN1CCC(CC1)N Request for Quotation
Chemical Name: 1-(2-fluoroethyl)piperidin-4-amine
CAS Number: 947263-70-9
Product Number: AG00IIHL(AGN-PC-015BEW)
Synonyms:
MDL No:
Molecular Formula: C7H15FN2
Molecular Weight: 146.2058032

Identification/Properties

Computed Properties
Molecular Weight:
146.209g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
146.122g/mol
Monoisotopic Mass:
146.122g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
89.6
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


1-(2-Fluoroethyl)piperidin-4-amine, also known as $name$, is a versatile compound that finds crucial application in chemical synthesis. With its unique chemical structure, this compound serves as a valuable building block in the creation of various advanced organic molecules. In particular, it is frequently employed as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and specialty chemicals.One of the primary functions of 1-(2-Fluoroethyl)piperidin-4-amine in chemical synthesis is as a precursor for the preparation of diverse heterocyclic compounds. By utilizing its specific functional groups and reactivity, chemists can efficiently introduce additional substituents and tailor the molecular structure to achieve desired properties. This compound plays a pivotal role in the construction of complex molecules with enhanced biological activity or improved performance characteristics.Moreover, 1-(2-Fluoroethyl)piperidin-4-amine serves as a valuable starting material for the synthesis of various pharmacologically active substances. By incorporating this compound into the synthesis route, researchers can access novel drug candidates, potential therapeutic agents, and innovative chemical entities. Its strategic placement in synthetic pathways enables the efficient production of diverse pharmaceutical intermediates and final products.Overall, the application of 1-(2-Fluoroethyl)piperidin-4-amine in chemical synthesis demonstrates its significance as a versatile and indispensable building block for the generation of valuable organic compounds. Chemists leverage its unique properties and functional groups to enable the efficient creation of complex molecules with diverse applications in pharmaceuticals, agrochemicals, and specialty chemicals.