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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)-

[2,2'-Bipyridine]-4,4'-dicarboxylic acid, diethyl ester

CCOC(=O)c1ccnc(c1)c1nccc(c1)C(=O)OCC Request for Quotation
Chemical Name: [2,2'-Bipyridine]-4,4'-dicarboxylic acid, diethyl ester
CAS Number: 1762-42-1
Product Number: AG0024H0(AGN-PC-0NHQXK)
Synonyms:
MDL No:
Molecular Formula: C16H16N2O4
Molecular Weight: 300.3092

Identification/Properties

Computed Properties
Molecular Weight:
300.314g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
7
Exact Mass:
300.111g/mol
Monoisotopic Mass:
300.111g/mol
Topological Polar Surface Area:
78.4A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
352
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Diethyl [2,2'-bipyridine]-4,4'-dicarboxylate is a versatile ligand utilized in chemical synthesis for its unique properties. In coordination chemistry, this compound is valued for its ability to bind to metal ions and facilitate various catalytic reactions. Its complex structure offers chelating capabilities, enabling the formation of stable coordination complexes with transition metals.One prominent application of Diethyl [2,2'-bipyridine]-4,4'-dicarboxylate is in the field of organic synthesis, where it serves as a key component in the preparation of metal-organic frameworks (MOFs) and coordination polymers. By acting as a bridging ligand between metal centers, it can influence the structure and properties of the resulting materials, making it an essential building block in supramolecular chemistry.Furthermore, the presence of the bipyridine moiety in Diethyl [2,2'-bipyridine]-4,4'-dicarboxylate imparts redox activity to the ligand, enabling it to participate in electron-transfer processes in electrocatalysis and photochemical reactions. This feature expands the scope of its synthetic applications, allowing for the design of new functional materials with potential applications in energy storage and conversion.Overall, the versatility of Diethyl [2,2'-bipyridine]-4,4'-dicarboxylate in chemical synthesis makes it a valuable tool for researchers seeking to develop novel catalysts, materials, and molecular structures with tailored properties and functionalities.