69010-90-8

Basic information

• Product Name: Ethanediamide,N1,N2-bis(2-furanylmethyl)-
• Synonyms: Ethanediamide,N,N'-bis(2-furanylmethyl)- (9CI); Oxamide, N,N'-difurfuryl- (7CI); NSC 320224
• CAS NO: 69010-90-8
• Molecular Formula: C12H12 N2 O4
• Molecular Weight: 248.238
• Mol File: 69010-90-8.mol
• Article Data: 7

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: 1.283g/cm³
• CAS DataBase Reference: Ethanediamide,N1,N2-bis(2-furanylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanediamide,N1,N2-bis(2-furanylmethyl)-(69010-90-8)
• EPA Substance Registry System: Ethanediamide,N1,N2-bis(2-furanylmethyl)-(69010-90-8)

Safety Data

• Hazardous Substances Data: 69010-90-8(Hazardous Substances Data)

Usage

General Description

Ethanediamide,N1,N2-bis(2-furanylmethyl)-, also known as bis(furan-2-ylmethyl)ethanediamide, is a chemical compound with the molecular formula C12H14N2O2. It is a polyamide derivative and belongs to the class of organic compounds known as furan derivatives. Ethanediamide,N1,N2-bis(2-furanylmethyl)- is used as a crosslinking agent which can be used to enhance the physical properties of a material or to increase the chemical resistance and durability of a material. It is commonly used as a curing agent in the production of epoxy resins and as a crosslinking agent for polymers. Additionally, it is known for its high thermal stability and resistance to high temperatures, making it a valuable component in the manufacturing of heat-resistant materials.

Upstream product

• 617-89-0 furan-2-ylmethanamine 
• 205749-77-5 methyl 2-((furan-2-ylmethyl)amino)-2-oxoacetate 
• 107-21-1 ethylene glycol 
• 79-37-8 oxalyl dichloride 

Downstream Products

• 617-89-0 furan-2-ylmethanamine 

Relevant articles and documents

Copper-Catalyzed Ullmann-Type Coupling and Decarboxylation Cascade of Arylhalides with Malonates to Access α-Aryl Esters

We have developed a high-efficiency and practical Cu-catalyzed cross-coupling to directly construct versatile α-aryl-esters by utilizing readily available aryl bromides (or chlorides) and malonates. These gram-scale approaches occur with turnovers of up to 1560 and are smoothly conducted by the usage of a low catalyst loading, a new available ligand, and a green solvent. A variety of functional groups are tolerated, and the application occurs with α-aryl-esters to access nonsteroidal anti-inflammatory drugs (NSAIDs) on the gram scale.

Synthesis of oxalamides by acceptorless dehydrogenative coupling of ethylene glycol and amines and the reverse hydrogenation catalyzed by ruthenium

A sustainable, new synthesis of oxalamides, by acceptorless dehydrogenative coupling of ethylene glycol with amines, generating H2, homogeneously catalyzed by a ruthenium pincer complex, is presented. The reverse hydrogenation reaction is also accomplished using the same catalyst. A plausible reaction mechanism is proposed based on stoichiometric reactions, NMR studies, X-ray crystallography as well as observation of plausible intermediates.

Copper(I) Oxide/N,N′-Bis[(2-furyl)methyl]oxalamide-Catalyzed Coupling of (Hetero)aryl Halides and Nitrogen Heterocycles at Low Catalytic Loading

An easily prepared oxalic diamide is a powerful ligand for the copper-catalyzed coupling of aryl halides with nitrogen heterocycles. Only 1–2 mol% each of copper(I) oxide and N,N′-bis[(2-furyl)methyl]oxalamide (BFMO) are needed to form N-arylation products under mild conditions. More than 10 different types of nitrogen heterocycles are compatible with these conditions, thereby giving the corresponding N-arylation products. (Figure presented.).