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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)-

1-O-tert-butyl 4-O-ethyl 4-pyridin-4-ylpiperidine-1,4-dicarboxylate

CCOC(=O)C1(CCN(CC1)C(=O)OC(C)(C)C)c1ccncc1 Request for Quotation
Chemical Name: 1-O-tert-butyl 4-O-ethyl 4-pyridin-4-ylpiperidine-1,4-dicarboxylate
CAS Number: 954125-18-9
Product Number: AG00IJ19(AGN-PC-0COV5Z)
Synonyms:
MDL No:
Molecular Formula: C18H26N2O4
Molecular Weight: 334.4100

Identification/Properties

Computed Properties
Molecular Weight:
334.416g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
334.189g/mol
Monoisotopic Mass:
334.189g/mol
Topological Polar Surface Area:
68.7A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
444
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#:
N/A
Hazard Statements:
H302-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


1-tert-Butyl 4-ethyl 4-(pyridin-4-yl)piperidine-1,4-dicarboxylate is a versatile compound that finds extensive utility in chemical synthesis, particularly in the field of medicinal chemistry. This compound serves as a key building block in the development of novel pharmaceutical agents due to its unique structural features and functional groups. In chemical synthesis, 1-tert-Butyl 4-ethyl 4-(pyridin-4-yl)piperidine-1,4-dicarboxylate can be utilized as a precursor for the synthesis of various heterocyclic compounds through organic transformations such as esterification, amidation, and cyclization reactions. Additionally, this compound can participate in multicomponent reactions to generate structurally diverse molecules with potential biological activity. Its presence in the molecular structure imparts desirable properties and enhances the pharmacological profile of the final molecules, making it an indispensable tool in the design and synthesis of new drug candidates and research chemicals.