58174-51-9

Upstream product

• 29305-46-2 4-(2,5-dioxo-2,5-dihydro-1-pyrrol-1-yl)benzoyl chloride 
• 17057-04-4 N-(4-carboxyphenyl)maleimide 
• 5432-04-2 N-(4-carboxyphenyl)maleamic acid 

Downstream Products

• 123457-83-0 4-(maleinimido)phenyl isocyanate 
• 756902-09-7 N-[p-(2-furfuryl-carbamate)phenylene]maleimide 

Relevant academic research and scientific papers

Organogelation behavior, thermal and mechanical properties of polymer network formed by the Diels-Alder reaction of furan- and maleimide-terminated four-arm star-shaped ε-caprolactone oligomers

Furan- and maleimide-terminated 4-arm star-shaped ε-caprolactone oligomers (F4CLO and M4CLO) were synthesized by the reactions of hydroxy-terminated 4-arm star-shaped ε-caprolactone oligomers (H4CLO) having the degree of polymerization per one oligocaprol

Bio-based thermosetting resins composed of aliphatic polyol-derived polymaleimides and allyleugenol

Bio-based bismaleimide (2MPD), trismaleimide (3MGC) and tetramaleimide (4MDG) were synthesized by reactions of 4-isocyanatophenylmaleimide with 1,3-propanediol, glycerol and α,α′-diglycerol, respectively. Although 2MPD did not melt until the temperature w

Selectivity control by chemical modification of the recognition sites in two-point binding molecularly imprinted polymer

We demonstrated the possibility of modifying the selectivity of a two-point binding imprinted polymer by chemical modification of the binding sites inside the cavities. We used a thermally reversible bond for the preparation of the monomer-template complex, which allowed us to remove the template easily by means of a simple thermal reaction and to simultaneously introduce various functional groups into the cavity. A phenylmaleimide having an azidocarbonyl group was reacted with diethylstilbestrol (DES, template) to yield a monomer, where the template was linked to two polymerizable maleimido groups via a thermally reversible urethane bond. The polymerization of the monomer was carried out in the presence of ethylene glycol dimethacrylate (EGDMA) by the initiation with 2,2-azobis(isobutyronitrile) (AIBN) at 54°C in DMF. The polymers were refluxed in 1,4-dioxane in the presence of a nucleophile such as water, methanol, or aniline. In this extraction step, the template molecules were removed from the polymer matrix, and simultaneously the isocyanato groups, which were generated by the thermal cleavage of the urethane bond, were converted to amino, urethane, or urea groups through their reaction with water, methanol, or aniline, respectively. The specific recognition ability of the imprinted polymers for the template and its structural analogues was dependent on the space between the two binding points as well as on the nature of the functional group. This method is especially propitious for developing artificial receptors for molecules lacking strongly interactive groups.

Ab-monomers. I: Synthesis and polymerization of furyl-maleimide monomers

New AB-monomers containing either furyl and maleimide groups or hydroxy and acid groups were prepared by the reaction of 4-maleimidobenzoic acid chloride or 4-maleimidophenylisocyanate with 2-furfuryl alcohol or the Diels-Alder reaction of 4-maleimidobenzoic acid with 2-furfuryl alcohol, respectively. The structures of the monomers were confirmed by IR, 1H-NMR and elemental analysis. By Diels-Alder polymerization reaction or polycondensation reaction new poly(esther-imide) or poly(urethane-imide)s were prepared. Thermal curing behavior of monomers was investigated by DSC analysis. All polymers were characterized by elemental analysis, IR spectral studies and thermogravimetry.

Synthesis and properties of a new selective bifunctional cross linking reagent

A new bifunctional reagent, 2 hydroxy 4 maleimidobenzoylazide, has been synthesised to serve as a selective agent for the step wise cross linking of mercapto and amino functions of proteins. The optimal reaction conditions and rate constants fo this reagent have been determined using model substances.