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BFMO

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[1][2].

Product Specifications

CAS Number

69010-90-8

Product Name Alternative

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

UNSPSC

12352200

Hazard Statement

H302, H315, H319, H335

Target

Biochemical Assay Reagents

Type

Biochemical Assay Reagents

Related Pathways

Others

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/bfmo.html

Purity

99.84

Solubility

10 mM in DMSO

Smiles

O=C(C(NCC1=CC=CO1)=O)NCC2=CC=CO2

Molecular Formula

C12H12N2O4

Molecular Weight

248.24

Precautions

H302, H315, H319, H335

References & Citations

[1]Bhunia S, et al. N, N'-Bisoxalamides Enhance the Catalytic Activity in Cu-Catalyzed Coupling of (Hetero) Aryl Bromides with Anilines and Secondary Amines. J Org Chem. 2017 Dec 1;82 (23) :12603-12612.|[2]Hu F, et al. Roles of naturally occurring biogenic iron-manganese oxides (BFMO) in PMS-based environmental remediation: A complete electron transfer pathway. J Environ Sci (China) . 2025 Sep;155:795-805.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Biochemical Assay Reagents

Clinical Information

No Development Reported

Available Sizes

Frequently Asked Questions

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