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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, 1-(4-piperidinylmethyl)-

C1CCN(CC1)CC1CCNCC1 Request for Quotation
Chemical Name: Piperidine, 1-(4-piperidinylmethyl)-
CAS Number: 32470-52-3
Product Number: AG00BYOO(AGN-PC-0NKCMW)
Synonyms:
MDL No:
Molecular Formula: C11H22N2
Molecular Weight: 182.3058

Identification/Properties

Computed Properties
Molecular Weight:
182.311g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
182.178g/mol
Monoisotopic Mass:
182.178g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
135
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-Piperidinylmethyl)piperidine is a versatile compound widely used in chemical synthesis as a key building block. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Specifically, it is utilized as a valuable intermediate in the synthesis of complex organic molecules due to its unique chemical structure and reactivity.In organic synthesis, 1-(4-Piperidinylmethyl)piperidine serves as a vital starting material for the construction of more intricate molecules through multistep reactions. Its piperidine ring provides a stable structural framework, while the attached piperidinylmethyl group offers a site for further functionalization and manipulation. This enables chemists to easily introduce specific functional groups or modify the compound to achieve desired properties in the final product.Moreover, the presence of both a tertiary amine and a secondary amine in the molecule enhances its utility in forming diverse chemical bonds and facilitating key transformations in synthetic pathways. This compound's structural features make it highly valuable in medicinal chemistry for the development of potential drug candidates with desired pharmacological activities.Overall, the application of 1-(4-Piperidinylmethyl)piperidine in chemical synthesis highlights its significance as a crucial building block that enables the efficient and strategic design of sophisticated organic molecules with broad industrial and scientific applications.