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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)-

tert-butyl 2-piperidin-4-ylpyrrolidine-1-carboxylate

O=C(N1CCCC1C1CCNCC1)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 2-piperidin-4-ylpyrrolidine-1-carboxylate
CAS Number: 929974-12-9
Product Number: AG00IHFJ(AGN-PC-00UYK4)
Synonyms:
MDL No:
Molecular Formula: C14H26N2O2
Molecular Weight: 254.3684

Identification/Properties

Computed Properties
Molecular Weight:
254.374g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
254.199g/mol
Monoisotopic Mass:
254.199g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
293
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


An essential compound in chemical synthesis, tert-Butyl 2-(piperidin-4-yl)pyrrolidine-1-carboxylate serves as a versatile building block with a myriad of applications. It acts as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural attributes and reactivity. By incorporating this compound into synthetic routes, chemists can access diverse molecular frameworks and facilitate the creation of complex organic molecules. Its strategic placement within a synthetic pathway enables the efficient construction of fused heterocyclic motifs and functionalized derivatives, paving the way for the development of novel compounds with potential biological activities. Leveraging the versatility of tert-Butyl 2-(piperidin-4-yl)pyrrolidine-1-carboxylate empowers chemists to tailor chemical structures for specific applications, making it a valuable tool in the realm of chemical synthesis.