38439-93-9

Usage

Uses

Used in Pharmaceutical Industry:
2,5-DIMETHOXYBENZENE-1,4-DIACETONITRILE is used as a precursor for the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows it to be a versatile building block in the development of new drugs and organic materials.
Used in Research and Development Laboratories:
In research and development settings, 2,5-DIMETHOXYBENZENE-1,4-DIACETONITRILE is used as a key intermediate in organic synthesis. It serves as a fundamental component in the creation of complex organic molecules, contributing to the advancement of chemical research and the discovery of novel compounds.
It is crucial to note that due to the potential health and safety risks associated with 2,5-DIMETHOXYBENZENE-1,4-DIACETONITRILE, proper protective equipment and handling procedures must be strictly adhered to when working with 2,5-DIMETHOXYBENZENE-1,4-DIACETONITRILE.

Upstream product

• 3752-97-4 1,4-bis(chloromethyl)-2,5-dimethoxybenzene 
• 151-50-8 potassium cyanide 
• 50874-27-6 1,4-bis(bromomethyl)-2,5-dimethoxybenzene 
• 150-78-7 1,4-dimethoxybezene 
• 143-33-9 sodium cyanide 

Downstream Products

• 38439-92-8 2-[4-(carboxymethyl)-2,5-dimethoxyphenyl]acetic acid 
• 5488-16-4 2,2′-(2,5-dihydroxy-1,4-phenylene)diacetic acid 
• 40995-65-1 1,4-bis(2-amino-1-ethyl)-2,5-dimethoxybenzene 
• 21172-01-0 Dimethyl-α,α,α'α'-tetracyano-2,5-dimethoxy-1,4-phenylendiacetat 
• 18389-97-4 11,11,12,12-tetracyano-1,4-naphthoquinodimethan 
• 56403-70-4 2,5-Dibromo-7,7,8,8-tetracyano-p-quinodimethane 
• 21003-99-6 2,5-dimethoxy-7,7,8,8-tetracyano-p-quinodimethane 
• 96802-43-6 2-(4-Dicyanomethyl-2,5-dimethoxy-phenyl)-malononitrile 
• 5628-25-1 2,5-bis(ethoxycarbonylmethyl)-1,4-bismethoxybenzene 
• 169522-50-3 2,5-bis-(2-amino-ethyl)-hydroquinone 
• 20452-46-4 (3,6-dioxo-cyclohexa-1,4-diene-1,4-diyl)-di-acetic acid 
• 5628-31-9 2,5-Bis-(ethoxycarbonylmethyl)-benzochinon 
• 51053-93-1 2,5-Dimethoxy-1,4-phenylendiacetylchlorid 
• 106591-96-2 methyl 2-[2,5-dimethoxy-4-(2-methoxy-2-oxoethyl)phenyl]acetate 

Relevant academic research and scientific papers

Ruthenium-catalyzed knoevenagel condensation: A new route toward cyano-substituted poly(p-phenylenevinylene)s

The ruthenium-catalyzed Knoevenagel reaction was developed for the preparation of cyano-substituted conjugated polymers. The polymerization was quenched by pouring the reaction mixture into methanol. The structures of polymers were confirmed by spectroscopic studies and elemental analysis. The results show that Knoevenagel polycondensation mediated by transition metal complexes enjoys the advantages of neutral and mild reaction conditions.