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1152979-47-9

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1152979-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1152979-47-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,2,9,7 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1152979-47:
(9*1)+(8*1)+(7*5)+(6*2)+(5*9)+(4*7)+(3*9)+(2*4)+(1*7)=179
179 % 10 = 9
So 1152979-47-9 is a valid CAS Registry Number.

1152979-47-9Relevant academic research and scientific papers

Synthesis and biological activities of novel 1,3,4-thiadiazole-containing pyrazole oxime derivatives

Dai, Hong,Li, Gang,Chen, Jia,Shi, Yujun,Ge, Shushan,Fan, Chongguang,He, Haibing

, p. 3818 - 3821 (2016)

A new library of 1,3,4-thiadiazole-containing pyrazole oximes was designed and synthesized. Their acaricidal and insecticidal activities were evaluated. Bioassay results indicated that some target compounds exhibited good acaricidal and insecticidal properties. Especially, compound 8m had 80% acaricidal activity against Tetranychus cinnabarinus at the concentration of 50?μg/mL, compound 8f displayed 100% insecticidal activities against Aphis craccivora at the concentration of 50?μg/mL, compounds 8r and 8w showed 100% insecticidal activities against Plutella xylostella at the concentration of 50?μg/mL. Furthermore, compounds 8r (LC50?=?19.61?μg/mL) and 8w (LC50?=?9.78?μg/mL) possessed comparable or even better insecticidal activities than the control Pyridalyl (LC50?=?17.40?μg/mL) against P. xylostella.

The thiazoylmethoxy modification on pyrazole oximes: Synthesis and insecticidal biological evaluation beyond acaricidal activity

Dai, Hong,Xiao, Yan-Shuang,Li, Zhong,Xu, Xiao-Yong,Qian, Xu-Hong

, p. 1014 - 1016 (2014/08/18)

A series of new pyrazole oximes bearing substituted thiazole ring were designed and prepared. The structures of the title compounds were identified by spectral analyses. The results of primary bioassay indicated that some targeted compounds exhibited promising insecticidal activity besides acaricidal activity, particularly; compounds 8c and 8d were more potent against Tetranychus cinnabarinus and Plutella xylostella than other analogues.

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