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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-methoxyphenyl)methyl]-

COc1ccc(cc1)CC1CCNCC1 Request for Quotation
Chemical Name: Piperidine, 4-[(4-methoxyphenyl)methyl]-
CAS Number: 37581-26-3
Product Number: AG0078OH(AGN-PC-0KZAMZ)
Synonyms:
MDL No: MFCD05863571
Molecular Formula: C13H19NO
Molecular Weight: 205.2961

Identification/Properties

Computed Properties
Molecular Weight:
205.301g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
205.147g/mol
Monoisotopic Mass:
205.147g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
169
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


4-(4-METHOXY-BENZYL)-PIPERIDINE is a versatile intermediate compound commonly used in chemical synthesis processes. This compound plays a crucial role in the production of various organic compounds due to its unique chemical properties and structural features.One of the key applications of 4-(4-METHOXY-BENZYL)-PIPERIDINE is in the synthesis of pharmaceuticals. It serves as a fundamental building block in the creation of medications and drugs, particularly those that target central nervous system disorders or neurological conditions. This compound's piperidine ring structure is essential for the development of therapeutic agents with specific pharmacological properties.Furthermore, 4-(4-METHOXY-BENZYL)-PIPERIDINE is extensively utilized in the synthesis of complex organic molecules such as heterocyclic compounds, natural products, and advanced materials. Its functional groups and reactivity make it a valuable tool for chemists in designing and constructing intricate molecular structures with precise control over stereochemistry and substitution patterns.Overall, the significance of 4-(4-METHOXY-BENZYL)-PIPERIDINE in chemical synthesis lies in its ability to serve as a versatile intermediate for the efficient and strategic assembly of diverse organic compounds, particularly in the development of pharmaceuticals and specialized materials.