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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)-

Carbamic acid, (2-oxo-3-piperidinyl)-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)NC1CCCNC1=O Request for Quotation
Chemical Name: Carbamic acid, (2-oxo-3-piperidinyl)-, 1,1-dimethylethyl ester
CAS Number: 99780-98-0
Product Number: AG003I6J(AGN-PC-0398CI)
Synonyms:
MDL No: MFCD13190662
Molecular Formula: C10H18N2O3
Molecular Weight: 214.2615

Identification/Properties

Properties
BP:
405.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
214.265g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
214.132g/mol
Monoisotopic Mass:
214.132g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
258
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tert-Butyl (2-oxopiperidin-3-yl)carbamate, commonly referred to as $name$, is a versatile compound that finds wide applications in chemical synthesis. This compound serves as a key building block in the preparation of various pharmaceuticals and agrochemicals. Due to its unique structural features, $name$ can be used for the synthesis of complex molecules with specific biological activities.In organic synthesis, $name$ is frequently employed as a protecting group for amines, enabling selective functionalization of other reactive sites within a molecule. By utilizing the reactivity of the carbamate functional group, chemists can introduce desired substituents or modify the properties of target compounds with precision. Additionally, $name$ serves as a valuable precursor for the generation of diverse heterocyclic compounds through cyclization reactions, contributing to the synthesis of new drug candidates and biologically active molecules.Moreover, the presence of the tert-butyl group in $name$ imparts stability and enhances the overall efficiency of synthetic routes by facilitating purification processes and improving the isolation of products. This feature makes $name$ a preferred reagent in the development of synthetic strategies for complex molecular structures. In summary, the strategic incorporation of tert-Butyl (2-oxopiperidin-3-yl)carbamate in chemical synthesis enables chemists to access structurally diverse compounds for applications in pharmaceutical research, drug discovery, and materials science.