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3-undecylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132983-00-7

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132983-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132983-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,8 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132983-00:
(8*1)+(7*3)+(6*2)+(5*9)+(4*8)+(3*3)+(2*0)+(1*0)=127
127 % 10 = 7
So 132983-00-7 is a valid CAS Registry Number.

132983-00-7Downstream Products

132983-00-7Relevant academic research and scientific papers

Discovery of Lipophilic Bisphosphonates That Target Bacterial Cell Wall and Quinone Biosynthesis

Malwal, Satish R.,Chen, Lu,Hicks, Hunter,Qu, Fiona,Liu, Weidong,Shillo, Alli,Law, Wen Xuan,Zhang, Jianan,Chandnani, Neal,Han, Xu,Zheng, Yingying,Chen, Chun-Chi,Guo, Rey-Ting,Abdelkhalek, Ahmed,Seleem, Mohamed N.,Oldfield, Eric

, p. 2564 - 2581 (2019)

We report that alkyl-substituted bisphosphonates have activity against Bacillus anthracis Sterne (0.40 μg/mL), Mycobacterium smegmatis (1.4 μg/mL), Bacillus subtilis (1.0 μg/mL), and Staphylococcus aureus (13 μg/mL). In many cases, there is no effect of serum binding, as well as low activity against a human embryonic kidney cell line. Targeting of isoprenoid biosynthesis is involved with 74 having IC50 values of ~100 nM against heptaprenyl diphosphate synthase and 200 nM against farnesyl diphosphate synthase. B. subtilis growth inhibition was rescued by addition of farnesyl diphosphate, menaquinone-4 (MK-4), or undecaprenyl phosphate (UP), and the combination of MK-4 and UP resulted in a 25× increase in ED50, indicating targeting of both quinone and cell wall biosynthesis. Clostridioides difficile was inhibited by 74, and since this organism does not synthesize quinones, cell wall biosynthesis is the likely target. We also solved three X-ray structures of inhibitors bound to octaprenyl diphosphate and/or undecaprenyl diphosphate synthases.

Iron(III)-Catalyzed Ortho-Preferred Radical Nucleophilic Alkylation of Electron-Deficient Arenes

Yu, Fei,Wang, Ting,Zhou, Huan,Li, Yajun,Zhang, Xinhao,Bao, Hongli

supporting information, p. 6538 - 6541 (2017/12/26)

The untraditional iron-catalyzed, ortho-preferred, radical alkylation of electron-deficient (hetero)arenes is reported. A variety of electron-deficient arenes were shown to react with various primary alkyl sources, producing the alkylated (hetero)arenes in good yields. This reaction might be an alkyl radical, nucleophilic aromatic substitution reaction, rather than the traditional electrophilic Friedel-Crafts reaction. HOMO-LUMO analysis and DFT studies on the key transition states underlying the regioselectivity are consistent with the observed reactions and the conclusions.

Antipruritic composition

-

, (2008/06/13)

An antipruritic composition for an oral medicine, injection, and external medicine, comprising an effective amount of a chelated zinc (e.g., zinc picolinate) as an antipruritic agent.

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