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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 1-(piperidin-4-yl) piperidin-4-ylcarbamate

O=C(OC(C)(C)C)NC1CCN(CC1)C1CCNCC1 Request for Quotation
Chemical Name: tert-butyl 1-(piperidin-4-yl) piperidin-4-ylcarbamate
CAS Number: 878156-65-1
Product Number: AG00IES3(AGN-PC-0WALEG)
Synonyms:
MDL No:
Molecular Formula: C15H29N3O2
Molecular Weight: 283.4097

Identification/Properties

Computed Properties
Molecular Weight:
283.416g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
283.226g/mol
Monoisotopic Mass:
283.226g/mol
Topological Polar Surface Area:
53.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
314
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


tert-Butyl [1,4'-bipiperidin]-4-ylcarbamate is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals. Its sterically hindered tert-butyl group provides stability and enhances the compound's solubility in organic solvents. In chemical synthesis, tert-Butyl [1,4'-bipiperidin]-4-ylcarbamate acts as a protective group for amines, facilitating selective reactions at other functional groups. Furthermore, its bipiperidin moiety offers a rigid scaffold, enabling the precise control of stereochemistry in complex molecule assembly. Overall, tert-Butyl [1,4'-bipiperidin]-4-ylcarbamate plays a crucial role in the synthesis of advanced materials and bioactive compounds.