1373883-35-2

Upstream product

• 1373883-29-4 (S)-2-methoxy-N-(1-((2-methoxyphenyl)amino)-3-(4-nitrophenyl)-1-oxopropan-2-yl)benzamide 
• 1373883-30-7 (S)-2-hydroxy-N-(1-((2-hydroxyphenyl)amino)-3-(4-nitrophenyl)-1-oxopropan-2-yl)benzamide 
• 1373883-31-8 (S)-N-(3-(4-aminophenyl)-1-((2-hydroxyphenyl)amino)-1-oxopropan-2-yl)-2-hydroxybenzamide 
• 67083-40-3 1,3-dimethyl-5-nitrosobenzene 
• 1373883-27-2 (S)-tert-butyl (1-((2-methoxyphenyl)amino)-3-(4-nitrophenyl)-1-oxopropan-2-yl)carbamate 
• 1373883-28-3 (S)-2-amino-N-(2-methoxyphenyl)-3-(4-nitrophenyl)propanamide hydrochloride 
• 33305-77-0 Boc-Phe(p-NO₂)-OH 
• 90-04-0 2-methoxy-phenylamine 

Relevant academic research and scientific papers

Reversible heterochiral aggregation/dissociation of bis(2-hydroxyphenyl) diamides driven by UV/Vis irradiation

Light to dissolve: (R)- and (S)-diamides bearing a hydrogen-bonding framework (red in picture) and a trans-azobenzene unit (blue) form an insoluble heterochiral aggregate, which can be dissolved by photoisomerization of the azobenzene unit to the cis conformation by UV irradiation (365-nm). The insoluble aggregate was formed again by subsequent irradiation with visible light (>422-nm). The precipitation and dissolution is manifestly reversible. Copyright