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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-(1H-imidazol-1-yl)-

N1CCC(CC1)n1cncc1 Request for Quotation
Chemical Name: Piperidine, 4-(1H-imidazol-1-yl)-
CAS Number: 147081-85-4
Product Number: AG001EKI(AGN-PC-0NKXL4)
Synonyms:
MDL No:
Molecular Formula: C8H13N3
Molecular Weight: 151.2089

Identification/Properties

Computed Properties
Molecular Weight:
151.213g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
151.111g/mol
Monoisotopic Mass:
151.111g/mol
Topological Polar Surface Area:
29.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
121
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(1H-imidazol-1-yl)piperidine is a versatile compound that finds wide application in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. It is commonly utilized as a key intermediate in the synthesis of bioactive molecules due to its unique structural properties.In organic synthesis, 4-(1H-imidazol-1-yl)piperidine is often employed as a nucleophilic catalyst or as a ligand in transition metal-catalyzed reactions. Its flexible imidazole ring and piperidine moiety can participate in a range of chemical reactions, enabling the formation of complex molecules with specific pharmacological or biological activities.Additionally, this compound can act as a chelating agent, forming stable complexes with various metal ions that can influence the reactivity and selectivity of chemical transformations. Its ability to coordinate with metals makes it a valuable tool in the development of asymmetric synthesis methodologies and in the preparation of enantioenriched compounds.Overall, the unique characteristics of 4-(1H-imidazol-1-yl)piperidine make it a valuable asset in the realm of chemical synthesis, offering diverse opportunities for the construction of novel molecules with potential applications in medicine, agriculture, and other fields.