1309582-33-9

Basic information

• Product Name: 2-ethylsulfonyl-5-(4-chlorobenzyl)-1,3,4-oxadiazole
• Synonyms: 2-ethylsulfonyl-5-(4-chlorobenzyl)-1,3,4-oxadiazole
• CAS NO: 1309582-33-9
• Molecular Weight: 286.739
• Mol File: 1309582-33-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-ethylsulfonyl-5-(4-chlorobenzyl)-1,3,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ethylsulfonyl-5-(4-chlorobenzyl)-1,3,4-oxadiazole(1309582-33-9)
• EPA Substance Registry System: 2-ethylsulfonyl-5-(4-chlorobenzyl)-1,3,4-oxadiazole(1309582-33-9)

Safety Data

• Hazardous Substances Data: 1309582-33-9(Hazardous Substances Data)

Upstream product

• 93073-38-2 2-mercapto-5-(4-chlorobenzyl)-1,3,4-oxadiazole 
• 57676-51-4 2-(4-chlorophenyl)acetic hydrazide 
• 52449-43-1 (4-chloro-phenyl)-acetic acid methyl ester 
• 1356585-59-5 C₁₁H₁₁ClN₂OS 
• 1878-66-6 4-chlorophenylacetic Acid 

Relevant articles and documents

A banana root nematodes such prevention of sulfide sulfones compound and its preparation method and application (by machine translation)

The invention relates to a prevention of the banana root nematodes sulfide sulfones compound and its preparation method and application, it can be prepared into various agricultural conventional dosage forms. The compound and derivatives thereof can effectively control insect banana thread. (by machine translation)

Inhibition of tobacco bacterial wilt with sulfone derivatives containing an 1,3,4-oxadiazole moiety

A series of new sulfone compounds containing the 1,3,4-oxadiazole moiety were designed and synthesized. Their structures were identified by 1H and 13C nuclear magnetic resonance and elemental analyses. Antibacterial bioassays indicated that most compounds exhibited promising in vitro antibacterial bioactivities against tobacco bacterial wilt at 200 μg/mL. The relationship between structure and antibacterial activity was also discussed. Among the title compounds, 5′c, 5′h, 5′i, and 5′j could inhibit mycelia growth of Ralstonia solanacearum in vitro by approximately 50% (EC50) at 39.8, 60.3, 47.9, and 32.1 μg/mL, respectively. Among them, compound 5′j was identified as the most promising candidate due to its stronger effect than that of Kocide 3000 [Cu(OH)2] within the same concentration range. Field trials demonstrated that the control effect of compound 5′j against tobacco bacterial wilt was better than that of the commercial bactericide Saisentong. For the first time, the present work demonstrated that sulfone derivatives containing 1,3,4-oxadiazole can be used to develop potential bactericides for plants.