939980-69-5

Upstream product

• 15267-46-6 ethyl 2-(4-methylsulfanylphenoxy)acetate 
• 1073-72-9 4-hydroxythioanisole 

Downstream Products

• 939980-72-0 4-amino-5-{[4-(methylthio)phenoxy]methyl}-4H-1,2,4-triazole-3-thiol 
• 848143-84-0 5-{[4-(methylthio)phenoxy]methyl}-1,3,4-oxadiazole-2-thiol 
• 1071459-08-9 C₁₇H₁₆N₂O₃S 
• 1071459-01-2 2-(4-methylphenyl)-5-{[4-(methylthio)phenoxy]methyl}-1,3,4-oxadiazole 
• 1071459-05-6 2-(2-methoxyphenyl)-5-{[4-(methylthio)phenoxy]methyl}-1,3,4-oxadiazole 
• 930020-47-6 2-{[4-(methylthio)phenoxy]methyl}-5-phenyl-1,3,4-oxadiazole 
• 1071459-06-7 C₁₆H₁₄N₂O₃S 
• 1071459-02-3 C₁₆H₁₃ClN₂O₂S 
• 1071459-04-5 C₁₇H₁₆N₂O₂S 
• 1071459-09-0 C₁₈H₁₈N₂O₂S 
• 1071459-03-4 C₁₇H₁₆N₂O₂S 

Relevant academic research and scientific papers

Synthesis and larvicidal activity of 1,3,4-oxadiazole derivatives containing a 3-chloropyridin-2-yl-1H-pyrazole scaffold

Abstract: A new series of 1,3,4-oxadiazole derivatives with a 3-chloropyridin-2-yl-1H-pyrazole moiety was designed, synthesized, and characterized. The results of bioassay against Helicoverpa armigera and Plutella xylostella indicated that some of the synthesized compounds showed remarkable larvicidal activity. In particular, the LC50 values of the most active compounds against P. xylostella were 46.5, 23.9, and 13.9?mg/dm3, and against Helicoverpa armigera were 88.3 and 69.5?mg/dm3, the latter being slightly better than commercial chlorpyrifos (LC50 103.77?mg/dm3). Preliminary SAR was also discussed. Graphical abstract: [Figure not available: see fulltext.].

Tirfluoromethylpyridine oxadiazoles (ether)derivative and application thereof

The invention discloses an application of a tirfluoromethylpyridine oxadiazole (ether)derivative in a pesticide. A structure is shown as a general formula I, a compound shown in the general formula Ihas good insecticidal activity, and can be used for controlling insects such as diamondback moth and armyworm. The compound has excellent control effect for insects such as diamondback moth and armyworm, and also has control effect for the insects having resistance to the traditional pesticides, in addition, introduction of fluorine-containing groups such as tirfluoromethylpyridine and oxadiazoleas well as heterocyclic ring can enhance a rate for forming hydrogen bond effect between a compound and a target, and the activity of the compound is increased.

Synthesis and antimicrobial activities of some novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines carrying thioalkyl and sulphonyl phenoxy moieties

Thirty one new 6-aryl-3-{(4-substituted phenoxy) methyl}-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles (6a-s) and 6-aryl-3-{(4-substituted phenoxy methyl}-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines (7a-l) have been synthesized from 4-thioalkyl phenols (1a-b)

Synthesis and antimicrobial activities of some novel 1,3,4-oxadiazoles carrying alkylthio and alkylsulphonyl phenoxy moieties

A series of new 2-[(4-alkylthio/alkylsulfonyl phenoxy) methyl]-5- substituted-1,3,4-oxadiazoles 4a-y, 5a-h) have been synthesized from 4-alkylthio phenol (1a-b) through a multi-step reaction sequence. Compounds 1a-b reacted with ethyl chloroacetate to giv