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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-Propenoic acid, copper(2+) salt

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Chemical Name: 2-Propenoic acid, copper(2+) salt
CAS Number: 20074-76-4
Product Number: AG002CY7(AGN-PC-0QRNTI)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


Copper(II) acrylate is a versatile compound that finds wide application in chemical synthesis, particularly in organic chemistry. It serves as a valuable catalyst in various reactions due to its ability to activate multiple types of bonds, making it an essential tool for promoting efficient and selective transformations of organic compounds.In organic synthesis, Copper(II) acrylate is commonly used in coupling reactions, such as the Ullmann coupling and Sonogashira coupling, where it facilitates the formation of new carbon-carbon and carbon-heteroatom bonds. Additionally, it can act as a catalyst in oxidative coupling reactions, leading to the synthesis of complex organic molecules with high efficiency.Furthermore, Copper(II) acrylate plays a crucial role in cross-coupling reactions, enabling the construction of intricate molecular structures through the selective connection of different chemical moieties. Its ability to mediate both homocoupling and heterocoupling reactions provides chemists with a powerful tool for designing and synthesizing diverse organic compounds.Overall, the use of Copper(II) acrylate in chemical synthesis offers researchers and practitioners an effective way to expand the scope of organic transformations, accelerate reaction rates, and achieve high levels of control over the stereochemistry and regioselectivity of the products. Its versatile applications make it a valuable asset in the toolkit of synthetic chemists striving to unlock new pathways towards the development of novel materials and pharmaceuticals.