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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)-

Nickel, dibromobis(tributylphosphine)-

CCCCP(CCCC)CCCC.CCCCP(CCCC)CCCC.Br[Ni]Br Request for Quotation
Chemical Name: Nickel, dibromobis(tributylphosphine)-
CAS Number: 15242-92-9
Product Number: AG00AKLF(AGN-PC-0Q6D16)
Synonyms:
MDL No:
Molecular Formula: C24H54Br2NiP2
Molecular Weight: 623.1345

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Chemical Structure


Dibromobis(tributylphosphine)nickel is a versatile and highly effective catalyst used in various chemical synthesis reactions. This complex has shown remarkable efficiency in promoting cross-coupling reactions, particularly in the formation of carbon-carbon bonds. With its unique structure and properties, Dibromobis(tributylphosphine)nickel facilitates the coupling of a wide range of organic substrates, enabling the synthesis of complex molecules with high yield and selectivity. Furthermore, the use of this catalyst has been extended to the synthesis of pharmaceuticals, agrochemicals, and materials, showcasing its significant impact in modern organic chemistry.