59223-72-2

Upstream product

• 345-35-7 2-fluorobenzyl chloride 
• 105-53-3 diethyl malonate 

Downstream Products

• 91319-47-0 2-fluorophenylmethyl-(2-fluoro-5-methoxyphenylmethyl)acetic acid 
• 1643-26-1 3-(2-fluorophenyl)propionic acid 
• 76727-25-8 2-(2-fluorophenylmethyl)propane-1,3-diol 
• 1333257-44-5 5-chloro-6-(2-fluorobenzyl)-7-hydroxypyrazolo[1,5-a]pyrimidine-3-carbonitrile 
• 1333257-56-9 6-(2-fluorobenzyl)-5,7-dichloropyrazolo[1,5-a]pyrimidine-3-carbonitrile 
• 1310276-56-2 6-(2-fluorobenzyl)-5,7-dihydroxypyrazolo[1,5-a]pyrimidine-3-carbonitrile 
• 62558-10-5 α-(o-Fluorbenzyl)malonsaeure 
• 1290128-93-6 2-(2-fluorobenzyl)propane-1,3-diyl diacetate 
• 1290128-94-7 2-(2-fluoro-5-nitrobenzyl)propane-1,3-diyl diacetate 
• 91319-49-2 2-(2-fluorophenylmethyl)-2-(2-fluoro-5-methoxyphenylmethyl)ethanol 
• 91319-65-2 3-(2-fluorophenyl)-N-(t-butyl)propanamide 
• 76727-28-1 hydroxymethyl-3 chromanne 

Relevant academic research and scientific papers

Synthesis and insecticidal activity of mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety

Mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety were designed, synthesized, and evaluated for their insecticidal activity. Some of the title compounds showed remarkable insecticidal properties against Aphis craccivora. Compound I13 exhibited satisfactory insecticidal activity against A. craccivora. Meanwhile, label-free proteomics analysis of compound I13 treatment identified a total of 821 proteins. Of these, 35 proteins were up-regulated, whereas 108 proteins were down-regulated. Differential expressions of these proteins reflected a change in cellular structure and metabolism.

Substituted (arylalkoxybenzyl)aminopropanamide derivatives and process for their preparation

The invention provides new compounds of formula (I) STR1 wherein, subject to a proviso, n is zero or an integer of 1 to 3; each of R and R1, which may be the same or different, is hydrogen, halogen, trifluoromethyl or C1 -C4/su