1601472-95-0

Basic information

• Product Name: 3-bromo-1-(3-chloropyridin-2-yl)-N-(4-cyano-2-methyl-6-((2-(propylamino)ethyl)carbamoyl)phenyl)-1H-pyrazole-5-carboxamide
• Synonyms: 3-bromo-1-(3-chloropyridin-2-yl)-N-(4-cyano-2-methyl-6-((2-(propylamino)ethyl)carbamoyl)phenyl)-1H-pyrazole-5-carboxamide
• CAS NO: 1601472-95-0
• Molecular Weight: 544.838
• Mol File: 1601472-95-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-bromo-1-(3-chloropyridin-2-yl)-N-(4-cyano-2-methyl-6-((2-(propylamino)ethyl)carbamoyl)phenyl)-1H-pyrazole-5-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-1-(3-chloropyridin-2-yl)-N-(4-cyano-2-methyl-6-((2-(propylamino)ethyl)carbamoyl)phenyl)-1H-pyrazole-5-carboxamide(1601472-95-0)
• EPA Substance Registry System: 3-bromo-1-(3-chloropyridin-2-yl)-N-(4-cyano-2-methyl-6-((2-(propylamino)ethyl)carbamoyl)phenyl)-1H-pyrazole-5-carboxamide(1601472-95-0)

Safety Data

• Hazardous Substances Data: 1601472-95-0(Hazardous Substances Data)

Upstream product

• 500011-86-9 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid 
• 500011-92-7 5-bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid ethyl ester 
• 500011-91-6 5-bromo-2-(3-chloro-pyridin-2-yl)-3,4-dihydro-2H-pyrazole-3-carboxylic acid ethyl ester 
• 2402-77-9 2,3-dichloro-pyridine 
• 500011-88-1 ethyl 1-(3-chloropyridin-2-yl)-3-hydroxy-4,5-dihydro-1H-pyrazole-5-carboxylate 
• 22841-92-5 (3-chloro-2-pyridyl)hydrazine 
• 736995-64-5 2-(3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazol-5-yl)-8-methyl-4-oxo-4H-benzo[d][1,3]oxazine-6-carbonitrile 
• 111-39-7 N-propylethane-1,2-diamine 

Relevant articles and documents

Novel chlorantraniliprole derivatives as potential insecticides and probe to chlorantraniliprole binding site on ryanodine receptor

The lepidopteran pests such as diamondback moth are the regularly harmful pests of crops in the world, which brings enormous losses in crop production. Chlorantraniliprole is an anthranilic diamide insecticide registered for the control of lepidopteran pests with high insecticidal activity, however with uncertain binding site action target of chlorantraniliprole on ryanodine receptor, a series of new chlorantraniliprole derivatives were synthesized and the insecticidal activities of these compounds against diamondback moth were evaluated with chlorantraniliprole and indoxacarb as control. All compounds except 8h, 8p and 8t exhibited varying degree of activities against diamondback moth. Especially, compounds 8c, 8i, 8k and 8l displayed good insecticidal activities against diamondback moth and the activities are even better than that of indoxacarb during 72 h period. The Ki values of all synthesized compounds were calculated through autodocking program respectively. The relationship between calculation value of molecular docking and results of insecticidal activities indicated that the proposed specific receptor, the membrane-spanning domain protein of diamondback moth ryanodine receptor in our study might have chlorantraniliprole binding sites.