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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)-

Propanoic acid, 2,2-dimethyl-, silver(1+) salt

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Chemical Name: Propanoic acid, 2,2-dimethyl-, silver(1+) salt
CAS Number: 7324-58-5
Product Number: AGN-PC-0U2R47
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


Silver(I) pivalate is a versatile chemical reagent commonly used in various organic synthesis reactions. It serves as an efficient catalyst in a wide range of transformations, including cross-coupling reactions, C-H activation, cyclization reactions, and more. The unique properties of silver(I) pivalate make it particularly effective in promoting challenging bond formations and facilitating complex molecular rearrangements. Its ability to activate certain bonds and stabilize reaction intermediates greatly enhances the efficiency and selectivity of organic reactions. Moreover, silver(I) pivalate has shown promising results in asymmetric synthesis, enabling the enantioselective production of valuable chiral compounds. Its compatibility with a variety of substrates and reaction conditions makes it a valuable tool for synthetic chemists seeking to access novel chemical structures and functional groups.