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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-fluorophenyl)methyl]-, hydrochloride

Fc1ccc(cc1)CC1CCNCC1.Cl Request for Quotation
Chemical Name: Piperidine, 4-[(4-fluorophenyl)methyl]-, hydrochloride
CAS Number: 92822-03-2
Product Number: AG00IMLK(AGN-PC-009AYG)
Synonyms:
MDL No: MFCD03840140
Molecular Formula: C12H17ClFN
Molecular Weight: 229.7215

Identification/Properties

Computed Properties
Molecular Weight:
229.723g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
229.103g/mol
Monoisotopic Mass:
229.103g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
158
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(4-Fluorobenzyl)piperidine hydrochloride is a versatile chemical compound commonly used in chemical synthesis processes. This compound serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it particularly useful in the synthesis of complex organic molecules with specific biological activities.In chemical synthesis, 4-(4-Fluorobenzyl)piperidine hydrochloride can be employed as a key intermediate for the production of diverse compounds due to its ability to undergo various chemical transformations such as acylations, alkylations, and cross-coupling reactions. This versatile compound can be readily incorporated into different molecular frameworks, enabling the synthesis of new and structurally diverse chemical entities with potential applications in drug discovery, material science, and other research fields.Furthermore, the presence of the piperidine ring in the structure of 4-(4-Fluorobenzyl)piperidine hydrochloride imparts unique electronic and steric properties to the compound, which can be leveraged in the design and synthesis of bioactive molecules targeting specific biological pathways or receptors. Its selective functionalization at the 4-position provides opportunities for fine-tuning its properties and interactions with biological targets, making it a valuable tool in medicinal chemistry and drug development.Overall, the application of 4-(4-Fluorobenzyl)piperidine hydrochloride in chemical synthesis offers researchers and chemists a powerful platform for creating structurally diverse and biologically relevant compounds with potential applications across various scientific disciplines.