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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)-

Copper, bis(2,2,6,6-tetramethyl-3,5-heptanedionato-kO,kO')-

[O-]/C(=CC(=O)C(C)(C)C)/C(C)(C)C.[O-]/C(=CC(=O)C(C)(C)C)/C(C)(C)C.[Cu+2] Request for Quotation
Chemical Name: Copper, bis(2,2,6,6-tetramethyl-3,5-heptanedionato-kO,kO')-
CAS Number: 14040-05-2
Product Number: AG0039F0(AGN-PC-0PPK36)
Synonyms:
MDL No:
Molecular Formula: C22H38CuO4
Molecular Weight: 430.0807

Identification/Properties

Computed Properties
Molecular Weight:
432.104g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
431.222g/mol
Monoisotopic Mass:
431.222g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
505
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper, also known as copper(II) 2,2,6,6-tetramethyl-3,5-heptanedionate, is a versatile organometallic compound commonly utilized in chemical synthesis as a catalyst. This complex has found widespread application in various organic reactions due to its unique properties.In chemical synthesis, Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper serves as a Lewis acid catalyst, facilitating a range of transformations including but not limited to carbon-carbon bond formation, oxidation reactions, and cross-coupling reactions. Its high stability and reactivity make it an attractive choice for promoting challenging reactions while offering good control over the reaction pathways.One of the key advantages of using this copper complex in chemical synthesis is its ability to catalyze reactions under mild conditions, leading to enhanced efficiency and selectivity in the production of valuable organic compounds. Additionally, Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper has shown promising results in promoting asymmetric transformations, making it a valuable tool in the synthesis of enantiomerically enriched compounds.Overall, the use of Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper in chemical synthesis offers a reliable and cost-effective approach to accessing complex molecular scaffolds and functionalized products, making it a preferred catalyst in the toolkit of synthetic chemists.