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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]-, hydrobromide

Fc1ccc(cc1)CC1CCNCC1.Br Request for Quotation
Chemical Name: Piperidine, 4-[(4-fluorophenyl)methyl]-, hydrobromide
CAS Number: 193357-52-7
Product Number: AG00I2XV(AGN-PC-01YZ1N)
Synonyms:
MDL No:
Molecular Formula: C12H17BrFN
Molecular Weight: 274.1725

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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(4-Fluorobenzyl)piperidine hydrobromide is a versatile compound widely used in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as a crucial intermediate in the synthesis of complex molecules due to its unique structural attributes and reactivity.In organic synthesis, 4-(4-Fluorobenzyl)piperidine hydrobromide can participate in a range of reactions such as nucleophilic substitution, reduction, and cross-coupling reactions. Its piperidine ring provides a handle for further derivatization, allowing for the introduction of various functional groups to tailor the properties of the final product. Additionally, the presence of the fluorobenzyl group offers opportunities for selective transformations to direct the chemical reactions towards desired pathways.This compound's application in chemical synthesis extends to the development of new drug candidates, where it can be utilized to construct pharmacophores with specific biological activities. By incorporating 4-(4-Fluorobenzyl)piperidine hydrobromide into drug design strategies, chemists can access diverse chemical space and explore novel therapeutic targets for various diseases.Furthermore, in the field of agrochemical synthesis, this compound plays a crucial role in the creation of crop protection agents and pest control chemicals. Its structural versatility allows for the design of environmentally friendly and effective active ingredients that target specific agricultural pests while minimizing impact on non-target organisms and ecosystems.Overall, the use of 4-(4-Fluorobenzyl)piperidine hydrobromide in chemical synthesis highlights its importance as a key intermediate for the production of valuable compounds in pharmaceutical, agrochemical, and specialty chemical industries.