1260116-24-2

Upstream product

• 139-85-5 3,4-dihydroxybenzaldehyde 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 2609-49-6 diethyl p-nitrobenzylphosphonate 
• 99815-16-4 3,4-bis(tert-butyldimethylsilanyloxy)benzaldehyde 

Downstream Products

• 1260116-27-5 (E)-4-(3,4-bis(tert-butyldimethylsilyloxy)styryl)benzenamine 
• 1260116-06-0 (E)-5-(4-aminostyryl)benzene-1,3-diol 
• 1260116-07-1 C₁₅H₁₅NO₂ 
• 1260116-08-2 C₁₆H₁₅NO₃ 
• 1260116-09-3 (E)-1-(4-(3,4-dihydroxystyryl)phenyl)-3-phenylurea 
• 1260116-10-6 (E)-1-(4-(3,4-dihydroxystyryl)phenyl)-3-(4-methoxyphenyl)urea 
• 1260116-11-7 (E)-1-(4-aminophenyl)-3-(4-(3,4-dihydroxystyryl)phenyl)urea 
• 1260116-12-8 (E)-1-(4-(3,4-dihydroxystyryl)phenyl)-3-p-tolylurea 
• 1260116-13-9 (E)-1-(4-(3,4-dihydroxystyryl)phenyl)-3-(4-trifluoromethylphenyl) 
• 1260116-14-0 (E)-1-(4-(3,4-dihydroxystyryl)phenyl)-3-(4-fluorophenyl)urea 
• 1260116-15-1 (E)-1-(2,4-difluorophenyl)-3-(4-(3,4-dihydroxystyryl)phenyl)urea 
• 1260116-16-2 (E)-1-(4-chlorophenyl)-3-(4-(3,4-dihydroxystyryl)phenyl)urea 

Relevant academic research and scientific papers

A novel competitive class of α-glucosidase inhibitors: (E)-1-phenyl-3-(4-styrylphenyl)urea derivatives

Competitive glycosidase inhibitors are generally sugar mimics that are costly and tedious to obtain because they require challenging and elongated chemical synthesis, which must be stereo-and regiocontrolled. Here, we show that readily accessible achiral