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N-(4-chloro-2-(isopropylcarbamoyl)-6-methylphenyl)-1-(2-chloro-6-nitrophenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1527508-13-9

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1527508-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1527508-13-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,7,5,0 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1527508-13:
(9*1)+(8*5)+(7*2)+(6*7)+(5*5)+(4*0)+(3*8)+(2*1)+(1*3)=159
159 % 10 = 9
So 1527508-13-9 is a valid CAS Registry Number.

1527508-13-9Downstream Products

1527508-13-9Relevant academic research and scientific papers

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

Zhang, Xiulan,Li, Yuxin,Ma, Jinlong,Zhu, Hongwei,Wang, Baolei,Mao, Mingzhen,Xiong, Lixia,Li, Yongqiang,Li, Zhengming

, p. 186 - 193 (2014/01/17)

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.

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