116507-13-2

Upstream product

• 106-49-0 p-toluidine 
• 2689-65-8 5-iodofuran-2-carbaldehyde 
• 116507-09-6 N-(5-iodo-2-furfurylidene)-p-toluidine 

Downstream Products

• 116507-22-3 7-Iodo-3-p-tolyl-10-oxa-3-aza-tricyclo[5.2.1.0^1,5]dec-8-ene 
• 175603-42-6 ((E)-But-2-enyl)-(5-methoxy-furan-2-ylmethyl)-p-tolyl-amine 
• 175603-47-1 (5-Methoxy-furan-2-ylmethyl)-(3-methyl-but-2-enyl)-p-tolyl-amine 
• 116507-14-3 N-(5-methoxy-2-furfuryl)-p-toluidine 
• 116507-17-6 Allyl-(5-iodo-furan-2-ylmethyl)-p-tolyl-amine 

Relevant academic research and scientific papers

New substituted alkenyl-furfuryl-aryl amines: Synthesis and their characterization

Reaction of several N-(5-substituted-2-furfuryl)-p-toluidines with the appropriate substituted allyl bromide gave new examples of tertiary amines (3a-e, 4a-e) with unique capability to react spontaneously in a sense of intramolecular [4+2]cycloaddition (I

Studies in the Furan Series. 23. Preparation of some New 5-Substituted furfurylallylarylamines. Influence of Substituents on the Intramolecular Diels-Alder (IMDA) Reaction

Several new N-allyl-N-(5-substituted)-2-furfuryl-p-toluidines IIIa-e with Cl, Br, I, NO2 or CH3O groups in position 5 of the furan nucleus were prepared by allylation of the corresponding secondary furfurylarylamines.Both, electron withdrawing and releasi