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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-(cyclopentylamino)piperidine-1-carboxylate

O=C(N1CCC(CC1)NC1CCCC1)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(cyclopentylamino)piperidine-1-carboxylate
CAS Number: 812690-40-7
Product Number: AG004YPF(AGN-PC-06RU86)
Synonyms:
MDL No:
Molecular Formula: C15H28N2O2
Molecular Weight: 268.3950

Identification/Properties

Computed Properties
Molecular Weight:
268.401g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
268.215g/mol
Monoisotopic Mass:
268.215g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
298
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


The tert-butyl 4-(cyclopentylamino)piperidine-1-carboxylate is a versatile compound widely utilized in chemical synthesis for its unique properties and diverse applications. This compound acts as a valuable building block in the creation of various organic molecules due to its functional groups and structural stability.In organic synthesis, tert-butyl 4-(cyclopentylamino)piperidine-1-carboxylate is commonly employed as a reagent for the introduction of the cyclopentylamino group into target molecules. This allows chemists to modify the structure of compounds and enhance their biological activity or physical properties. The presence of the tert-butyl group also provides increased steric hindrance, which can influence the reactivity and selectivity of chemical reactions.Furthermore, the piperidine ring in this compound serves as a key scaffold in medicinal chemistry and drug discovery research. By incorporating tert-butyl 4-(cyclopentylamino)piperidine-1-carboxylate into the synthesis of pharmaceutical compounds, scientists can develop new drugs with enhanced potency, reduced side effects, and improved pharmacokinetic profiles.Overall, the application of tert-butyl 4-(cyclopentylamino)piperidine-1-carboxylate in chemical synthesis offers a powerful tool for the construction of complex organic molecules, facilitating the development of novel materials, pharmaceuticals, and other functional compounds.