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BFMO

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (1)

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-W054259

*BFMO* N,N'-Difurfuryloxamide; N1,N2-Bis(furan-2-ylmethyl)oxalamide	Biochemical Assay Reagents	Others
BFMO is a bidentate ligand for copper (Cu) catalysts that can effectively promote copper-catalyzed N-arylation coupling reactions of (hetero)aryl bromides with aniline, cyclic secondary amines, and acyclic secondary amines. BFMO coordinates with copper ions to form stable catalytically active species, which reduces the activation energy of the reaction and improves the reactivity of the substrate. It exhibits excellent selectivity for coupling of acyclic secondary amines with large steric hindrance, and can achieve direct monoarylation of piperazine with (hetero)aryl bromides to generate important pharmaceutical structural units .

Cat. No.	Product Name	Type

HY-W054259

*BFMO* N,N'-Difurfuryloxamide; N1,N2-Bis(furan-2-ylmethyl)oxalamide	Biochemical Assay Reagents
BFMO is a bidentate ligand for copper (Cu) catalysts that can effectively promote copper-catalyzed N-arylation coupling reactions of (hetero)aryl bromides with aniline, cyclic secondary amines, and acyclic secondary amines. BFMO coordinates with copper ions to form stable catalytically active species, which reduces the activation energy of the reaction and improves the reactivity of the substrate. It exhibits excellent selectivity for coupling of acyclic secondary amines with large steric hindrance, and can achieve direct monoarylation of piperazine with (hetero)aryl bromides to generate important pharmaceutical structural units .

BFMO

N,N'-Difurfuryloxamide; N1,N2-Bis(furan-2-ylmethyl)oxalamide

Biochemical Assay Reagents

BFMO is a bidentate ligand for copper (Cu) catalysts that can effectively promote copper-catalyzed N-arylation coupling reactions of (hetero)aryl bromides with aniline, cyclic secondary amines, and acyclic secondary amines. BFMO coordinates with copper ions to form stable catalytically active species, which reduces the activation energy of the reaction and improves the reactivity of the substrate. It exhibits excellent selectivity for coupling of acyclic secondary amines with large steric hindrance, and can achieve direct monoarylation of piperazine with (hetero)aryl bromides to generate important pharmaceutical structural units .

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BFMO

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Biochemical Assay Reagents