59574-37-7

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 1187-42-4 diaminomaleonitrile 

Downstream Products

• 88549-04-6 2-amino-3-<2-(p-methoxyphenyl)aziridin-1-yl>maleonitrile 
• 63857-93-2 2-(4-methoxyphenyl)-1H-imidazole-4,5-dicarbonitrile 
• 67170-60-9 5-(4-methoxyphenyl)pyrazine-2,3-dicarbonitrile 
• 37494-42-1 5-(4-methoxy-phenyl)-1,4,5,6-tetrahydro-pyrazine-2,3-dicarbonitrile 
• 66482-96-0 1-[(Z)-1,2-Dicyano-2-(4-methoxy-benzylamino)-vinyl]-3-isopropyl-urea 
• 68568-19-4 (Z)-2-Amino-3-cyano-3-{[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-amino}-acrylamide 

Relevant academic research and scientific papers

Revisiting the reaction between diaminomaleonitrile and aromatic aldehydes: A green chemistry approach

The reaction between diaminomaleonitrile (DAMN) and aldehydes and the resulting monoimines are well known. Since the standard reaction conditions involve the use of toxic solvents (typically methanol), we have sought to apply green chemistry principles to

Rapid synthesis of 2-amino maleonitrile Schiff bases in aqueous media catalyzed by cerium(IV) ammonium nitrate (CAN) and a new method for the one-pot preparation of their dicyano imidazoles (DCI)

A quick and simple method has been developed for the synthesis of 2-amino maleonitrile Schiff bases 3(a–k) through the reaction of 2,3-diaminomaleonitrile (DAMN) and aromatic aldehydes in the presence of catalytic amounts of cerium(IV) ammonium nitrate (C