1527508-09-3

Basic information

• Product Name: N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(2-chloro-6-nitrophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide
• Synonyms: N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(2-chloro-6-nitrophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide
• CAS NO: 1527508-09-3
• Molecular Weight: 516.263
• Mol File: 1527508-09-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(2-chloro-6-nitrophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(2-chloro-6-nitrophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide(1527508-09-3)
• EPA Substance Registry System: N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(2-chloro-6-nitrophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide(1527508-09-3)

Safety Data

• Hazardous Substances Data: 1527508-09-3(Hazardous Substances Data)

Upstream product

• 904733-74-0 5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazole 
• 904733-75-1 C₁₄H₇ClF₃N₃O₃ 
• 904733-76-2 C₁₁H₅ClF₃N₃O₄ 
• 890707-28-5 2-amino-3-methyl-5-chlorobenzoyl-N-methylamine 

Relevant articles and documents

Synthesis and insecticidal evaluation of novel anthranilic diamides containing N-substitued nitrophenylpyrazole

To cope with developing pest resistance and ecological problems associated with conventional insecticides and to search for potent insecticides targeting at ryanodine receptor (RyR), a series of novel anthranilic diamides containing N-substitued nitrophenylpyrazole were designed and synthesized. The insecticidal activities of target compounds against oriental armyworm (Mythimna separata) and diamondback moth (Plutella xylostella) were evaluated in our greenhouse by bio-assay tests and the relative structure-activity relationships were briefly discussed. Most compounds exhibited moderate to high activities, in which G 7 and K5 showed high activity against oriental armyworm and K2 and K4 against diamondback moth even better than the control-chlorantraniliprole. The calcium imaging technique was used to investigate the effects of several typical title compounds on the [Ca 2+]i, especially the effects of G7 on the intracellular calcium ion concentration ([Ca2+]i) in neurons, which indicated that some title compounds were potent activators of the RyR.