2795-61-1 Usage
Derivative of benzoic acid
2-fluorophenoxy group attached to the benzene ring The compound is derived from benzoic acid by attaching a 2-fluorophenoxy group to the benzene ring, which modifies its chemical properties and reactivity.
Use in pharmaceutical industry
Intermediate in the synthesis of various drugs and organic compounds 2-(2-fluorophenoxy)benzoic acid is commonly used as an intermediate in the production of different drugs and organic compounds, making it an important substance in the pharmaceutical industry.
Use as a building block
Production of agrochemicals, dyes, and other organic chemicals The compound is also used as a building block in the synthesis of agrochemicals, dyes, and other organic chemicals, highlighting its versatility in various industries.
Valuable tool for chemical research and development
Due to its properties 2-(2-fluorophenoxy)benzoic acid is a valuable tool in chemical research and development because of its unique properties, which can be exploited to create new compounds and materials.
Potential toxicity
Importance of handling with caution Since 2-(2-fluorophenoxy)benzoic acid has potential toxicity, it is crucial to handle it with care and follow proper safety precautions to avoid adverse effects on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 2795-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,9 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2795-61:
(6*2)+(5*7)+(4*9)+(3*5)+(2*6)+(1*1)=111
111 % 10 = 1
So 2795-61-1 is a valid CAS Registry Number.
2795-61-1Relevant articles and documents
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.
Tricyclic psychotropic agents containing two chalcogen atoms in the central ring: Synthesis of 11-(dimethylaminoalkyl) derivatives of 11H-dibenzo[b,e]-1,4-dioxepin and 11H-dibenzo[b,e]-1,4-dithiepin
Sindelar,Holubek,Ryska,et al.
, p. 72 - 87 (2007/10/02)
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