51597-76-3

Upstream product

• 95124-21-3 N-Furfurylidene-m-chloroaniline 
• 108-42-9 3-chloro-aniline 
• 617-89-0 furan-2-ylmethanamine 
• 98-01-1 furfural 

Downstream Products

• 95124-50-8 N-Allyl-N-furfuryl-m-chloroaniline 
• 95124-27-9 N-Furfuryl m-chloroaniline picrate 
• 95124-59-7 3-(3-Chloro-phenyl)-10-oxa-3-aza-tricyclo[5.2.1.0^1,5]dec-8-ene; compound with picric acid 
• 95124-53-1 N-Allyl-N-furfuryl-m-chloroaniline picrate 
• 95124-58-6 N-(m-Chlorophenyl)-5,7a-epoxy-4H-isoindoline 
• 95124-28-0 1-(3-Chloro-phenyl)-1-furan-2-ylmethyl-3-phenyl-thiourea 

Relevant academic research and scientific papers

Furfural and 5-(hydroxymethyl)furfural valorization using homogeneous Ni(0) and Ni(II) catalysts by transfer hydrogenation

The complex [dippeNi(COD)] (dippe =1,2-bis(diisopropyl phosphino)ethane) was used as a catalytic precursor in furfural (FF) and 5-(hydroxymethyl)furfural (HMF) valorization, along with formic acid as hydrogen transfer agent, to produce the corresponding a

Unsymmetrical indazolyl-pyridinyl-triazole ligand-promoted highly active iridium complexes supported on hydrotalcite and its catalytic application in water

Herein, an indazolyl-pyridinyl-triazole ligand was synthesized and its iridium complex supported on hydrotalcite was characterized via X-ray power diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray (EDX) spectroscopy and transmission electron microscopy (TEM). This new heterogeneous catalyst bearing the unsymmetrical indazolyl-pyridinyl-triazole ligand exhibits high catalytic activity in water. Both functionalized amines and imines were obtained from the challenging selective reaction of benzylamines with arylamines through transfer hydrogenation and dehydrogenation under clean conditions. In particular, it was observed that this catalyst system showed good recovery performance in water. Mechanistic studies showed that this transformation occurs via amine dehydrogenation, hydrolysis and condensation processes. The direct capture of the reaction intermediate provides sufficient proof for this process.

Preparative synthesis of 7-carboxy-2-R-isoindol-1-ones

A preparative method for the synthesis of 7-carboxy-2-R-isoindol-1-ones was developed on the basis of the [4+2] cycloaddition of secondary furfurylamines to maleic anhydride.

STUDIES IN THE FURAN SERIES. 22. N-ARYLFURFURYL- AND N-ARYL-5-METHYLFURFURYLAMINES AND THEIR N-ALLYL DERIVATIVES.

The compounds, where aryl is a meta- or para-substituted chlorophenyl, methoxyphenyl, or methylphenyl group, were prepared by reduction of corresponding azomethines. Their allylation with allyl iodide or allyl bromide yielded tertiary N-arylfurfurylamines