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2-(2-Fluoro-phenoxy)-benzoic acid methyl ester is a synthetic organic compound with the chemical formula C15H11FO3. It is a derivative of benzoic acid, featuring a methyl ester group and a 2-fluoro-phenoxy substituent. 2-(2-fluoro-phenoxy)-benzoic acid methyl ester is characterized by its aromatic structure, with a benzene ring bearing a fluorine atom at the para position and an ester-linked phenoxy group at the ortho position. It is used in various applications, including pharmaceuticals and agrochemicals, due to its potential biological activity. The compound's properties, such as its solubility and reactivity, can be influenced by the presence of the fluorine atom, which can affect its electronic and steric characteristics.

395-92-6

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395-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 395-92-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 395-92:
(5*3)+(4*9)+(3*5)+(2*9)+(1*2)=86
86 % 10 = 6
So 395-92-6 is a valid CAS Registry Number.

395-92-6Relevant academic research and scientific papers

Synthesis, fungicidal activity, and 3D-QSAR of tetrazole derivatives containing phenyloxadiazole moieties

Li, Yi-Tao,Yao, Wen-Qiang,Zhou, Si,Xu, Jun-Xing,Lu, Hui,Lin, Jian,Hu, Xiao-Yun,Zhang, Shao-Kai

, (2021/01/11)

In an effort to discover new agents with good fungicidal activities against CDM (cucumber downy mildew), a series of tetrazole derivatives containing phenyloxadiazole moieties were designed and synthesized. The EC50 values for fungicidal activities against CDM were determined. Bioassay results indicated that most synthesized compounds exhibited potential in vivo fungicidal activity against CDM. A CoMFA (comparative molecular field analysis) model based on the bioactivity was developed to identify some primary structural quality for the efficiency. The values of q2 and r2 for the established model were 0.791 and 0.982 respectively, which reliability and predict abilities were verified. Three analogues (q3, q4, q5) were designed and synthesized based on the model. All these compounds exhibited significant fungicidal activity on CDM with the EC50 of 1.43, 1.52, 1.77 mg·L?1. This work could provide a useful instruction for the further structure optimization.

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