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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 4-(cyclobutylamino)piperidine-1-carboxylate

O=C(N1CCC(CC1)NC1CCC1)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(cyclobutylamino)piperidine-1-carboxylate
CAS Number: 812690-41-8
Product Number: AG008KMO(AGN-PC-0BSBJ1)
Synonyms:
MDL No:
Molecular Formula: C14H26N2O2
Molecular Weight: 254.3684

Identification/Properties

Computed Properties
Molecular Weight:
254.374g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
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:
287
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


Tert-Butyl 4-(cyclobutylamino)piperidine-1-carboxylate is a versatile compound widely utilized in chemical synthesis. This compound serves as a key building block in the creation of complex molecules, particularly in the field of pharmaceuticals and material science. Its unique structure allows for strategic modifications, enabling chemists to introduce specific functional groups and stereochemistries into target molecules. By incorporating tert-Butyl 4-(cyclobutylamino)piperidine-1-carboxylate into synthetic pathways, researchers can access a diverse range of molecular frameworks with potential applications in drug discovery, agrochemicals, and advanced materials development. Additionally, the controlled reactivity and stability of this compound make it a valuable tool for designing efficient and sustainable synthetic routes in the laboratory.