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N,N'-dithio-bis(ethyl 3-(benzylamino)propanoate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95255-57-5

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95255-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95255-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,5 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 95255-57:
(7*9)+(6*5)+(5*2)+(4*5)+(3*5)+(2*5)+(1*7)=155
155 % 10 = 5
So 95255-57-5 is a valid CAS Registry Number.

95255-57-5Downstream Products

95255-57-5Relevant academic research and scientific papers

Design, synthesis, and insecticidal activities of new N-benzoyl-N'-phenyl- N'-sulfenylureas

Sun, Ranfeng,Zhang, Yonglin,Chen, Li,Li, Yongqiang,Li, Qingshan,Song, Haibin,Huang, Runqiu,Bi, Fuchun,Wang, Qingmin

experimental part, p. 3661 - 3668 (2010/06/19)

Aseries of new N'-alkylaminothio,N'-arylaminothio (or dithio), and N',N'-thio (or dithio) derivatives ofN'-benzoyl-N'-phenylureas were designed and synthesized as insect-growth regulators with sulfur dichloride or disulfur dichloride as the original reactant. The new compounds were identified by 1H nuclear magnetic resonancee (NMR) spectroscopy, elemental analysis [or high-resolution mass spectrometry (HRMS)], and single-crystal X-ray diffraction analysis. The X-ray results demonstrated that there exist N-S-N or N-S-S-N bonds in these new compounds. In comparison to the parent N-benzoyl-N'-phenylureas, these derivatives displayed better solubility. The insecticidal activities of the target compounds were evaluated. The results of bioassays showed that compounds 1-24 retained the larvicidal activities of the corresponding benzoylphenylureas (BPUs) and some compounds exhibited better larvicidal activities against oriental armyworm and mosquitoes than the parent BPUs. The larvicidal activities of the selected target compounds 1 and 24 against diamondback moth were better than that of the corresponding parent compounds E and triflumuron.

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