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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)-

ethyl 2,4-dioxo-4-pyridin-2-ylbutanoate

CCOC(=O)C(=O)CC(=O)c1ccccn1 Request for Quotation
Chemical Name: ethyl 2,4-dioxo-4-pyridin-2-ylbutanoate
CAS Number: 92288-93-2
Product Number: AG00GVVC(AGN-PC-0NHZQ6)
Synonyms:
MDL No: MFCD08056636
Molecular Formula: C11H11NO4
Molecular Weight: 221.2093

Identification/Properties

Computed Properties
Molecular Weight:
221.212g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
221.069g/mol
Monoisotopic Mass:
221.069g/mol
Topological Polar Surface Area:
73.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
288
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The Ethyl 2,4-dioxo-4-(pyridin-2-yl)butanoate is a versatile compound commonly utilized in chemical synthesis processes due to its unique properties. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and complex organic molecules. One of the primary applications of Ethyl 2,4-dioxo-4-(pyridin-2-yl)butanoate is in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. Its ability to undergo diverse chemical reactions makes it a valuable intermediate in the production of novel drugs with enhanced bioactivity and pharmacokinetic properties. Furthermore, this compound is employed in the preparation of specialized materials such as ligands for catalysis, fluorescent dyes, and molecular probes. Its structural features enable precise modifications that facilitate the design of functional molecules for specific applications in various industries. Overall, Ethyl 2,4-dioxo-4-(pyridin-2-yl)butanoate plays a crucial role in advancing chemical synthesis capabilities and expanding the scope of molecular design for cutting-edge research and development.