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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)-

dimethyl 2,5-dioxobicyclo[2.2.2]octane-1,4-dicarboxylate

COC(=O)C12CCC(C(=O)C1)(CC2=O)C(=O)OC Request for Quotation
Chemical Name: dimethyl 2,5-dioxobicyclo[2.2.2]octane-1,4-dicarboxylate
CAS Number: 174685-34-8
Product Number: AG001ZVB(AGN-PC-0730SG)
Synonyms:
MDL No:
Molecular Formula: C12H14O6
Molecular Weight: 254.2360

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


A notable application of Dimethyl 2,5-dioxobicyclo[2.2.2]octane-1,4-dicarboxylate in chemical synthesis is its role as a versatile building block in the creation of complex molecules and pharmaceutical compounds. This compound serves as a key intermediate in the synthesis of various organic molecules due to its unique structure and reactivity. By participating in a range of chemical reactions such as esterification, reduction, and functional group transformations, Dimethyl 2,5-dioxobicyclo[2.2.2]octane-1,4-dicarboxylate enables the efficient and selective formation of intricate molecular structures. Chemists leverage its scaffold to introduce specific functionalities and stereochemistries, making it a valuable tool in the synthesis of biologically active compounds and materials with tailored properties.