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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, 3-bromo-4-oxo-, ethyl ester

CCOC(=O)N1CCC(=O)C(C1)Br Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 3-bromo-4-oxo-, ethyl ester
CAS Number: 95629-02-0
Product Number: AG00IJ9L(AGN-PC-00O192)
Synonyms:
MDL No:
Molecular Formula: C8H12BrNO3
Molecular Weight: 250.0898

Identification/Properties

Computed Properties
Molecular Weight:
250.092g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
249g/mol
Monoisotopic Mass:
249g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
219
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


Ethyl 3-bromo-4-oxo-piperidine-1-carboxylate is a versatile chemical compound widely utilized in chemical synthesis for its valuable applications. This compound serves as a key building block in organic synthesis, particularly in the creation of pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, Ethyl 3-bromo-4-oxo-piperidine-1-carboxylate plays a crucial role as a precursor in the preparation of various biologically active molecules. Its unique structure and reactivity make it an essential intermediate in the development of pharmaceutical compounds, such as potential drug candidates and therapeutic agents.Furthermore, this compound is utilized in the construction of heterocyclic compounds and complex organic molecules, which are essential in the field of medicinal chemistry. Its functional groups enable diverse chemical transformations, allowing chemists to modify and functionalize the molecule to create new compounds with specific properties and activities.Overall, Ethyl 3-bromo-4-oxo-piperidine-1-carboxylate is a valuable tool in chemical synthesis, enabling scientists to access a wide range of functionalized compounds for various applications in drug discovery, materials science, and other areas of research and development.