1427296-24-9

Upstream product

• 20922-60-5 2,6-dimethylphenylcyanamide 
• 106-51-4 p-benzoquinone 

Downstream Products

• 1427296-31-8 3-(2,6-dimethylphenyl)-2-imino-2,3-dihydrobenzo[d]oxazol-5-yl 4-methylbenzenesulfonate 

Relevant academic research and scientific papers

Preparation of novel palladium nanoparticles supported on magnetic iron oxide and their catalytic application in the synthesis of 2-imino-3-phenyl-2,3-dihydrobenzo[d]oxazol-5-ols

Novel Pd nanoparticles were prepared in five successive stages: 1) preparation of the Fe3O4 magnetic nanoparticles (Fe3O4 MNPs), 2) coating of Fe3O4 MNPs with SiO2 (Fe3/sub

Biosynthesis of Cu/Fe3O4 nanoparticles using Alhagi camelorum aqueous extract and their catalytic activity in the synthesis of 2-imino-3-aryl-2,3-dihydrobenzo[d]oxazol-5-ol derivatives

A novel, low-cost and green method was developed for the synthesis of Cu/Fe3O4 nanoparticles (NPs) using Alhagi camelorum aqueous extract as a safe reducing agent and effective stabilizer without addition of any chemical reducing agents or surfactants. TEM (transmission electron microscopy), FT-IR (Fourier transform infrared spectroscopy), XRD (X-ray diffraction), FESEM (field emission scanning electron microscopy), EDS (energy-dispersive X-ray spectroscopy), and UV–Vis (ultraviolet visible) analyses were used for the characterization of green synthesized NPs. The FT-IR analysis confirmed the existence of different functional groups of Alhagi camelorum extract phytochemicals which were responsible for the fabrication of NPs. Finally, the magnetic Cu nanocatalyst was employed for the preparation of 2-imino-3-aryl-2,3-dihydrobenzo[d]oxazol-5-ol derivatives via the reaction of arylcyanamides and p-benzoquinone at ambient temperature. The biosynthesized Cu/Fe3O4 NPs can be recovered and reused for five cycles with no significant reduction of catalytic activity.

Ultrasound-promoted synthesis of novel 2-imino-3-aryl-2,3-dihydrobenzo[d] oxazol-5-ol 2-iminooxazolidines derivatives

A synthesis of novel 2-iminooxazolidineswas developed by the reaction between arylcyanamides with p-benzoquinone at room temperature under ultrasound irradiation in excellent yields. Also, the chemoselective tosylation of the products were performed at room temperature under ultrasound irradiation in good yields.