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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)-

1-Piperidinecarboxylic acid, 5-ethyl-2,4-dioxo-, 1,1-dimethylethyl ester

CCC1CN(C(=O)OC(C)(C)C)C(=O)CC1=O Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 5-ethyl-2,4-dioxo-, 1,1-dimethylethyl ester
CAS Number: 845267-80-3
Product Number: AG0053WT(AGN-PC-0IBHM7)
Synonyms:
MDL No:
Molecular Formula: C12H19NO4
Molecular Weight: 241.2836

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
241.287g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
241.131g/mol
Monoisotopic Mass:
241.131g/mol
Topological Polar Surface Area:
63.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
343
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


1-Boc-5-Ethyl-2,4-dioxopiperidine, also known as ethyl 5-boc-2,4-dioxopiperidine-1-carboxylate, is a versatile compound widely used in chemical synthesis. It serves as a valuable building block in the creation of complex molecules due to its unique structure and reactivity. In chemical synthesis, 1-Boc-5-Ethyl-2,4-dioxopiperidine is commonly employed as a protecting group for amines. By selectively masking the amino functionality with the Boc (tert-butyloxycarbonyl) group, this compound allows for the manipulation of other functional groups without affecting the amine group. This protection strategy is crucial in the controlled synthesis of various pharmaceuticals, natural products, and specialty chemicals.Moreover, 1-Boc-5-Ethyl-2,4-dioxopiperidine plays a key role in the construction of heterocyclic compounds, which are essential structural motifs found in numerous biologically active molecules. This compound's ability to facilitate cyclization reactions enables the formation of diverse ring systems with high efficiency and selectivity.Overall, the application of 1-Boc-5-Ethyl-2,4-dioxopiperidine in chemical synthesis is instrumental in streamlining complex molecule assembly, protecting key functional groups, and enabling the creation of structurally diverse and biologically relevant compounds.