825-60-5 Usage
Description
Benzimidic acid ethyl is a chemical compound that consists of a benzene ring fused to an imidazole ring, and is an ethyl ester derivative of benzimidazole-2-carboxylic acid. It is commonly used in pharmaceutical research and drug development due to its potential biological activities, such as antimicrobial, antiviral, and anti-inflammatory properties.
Used in Pharmaceutical Research and Drug Development:
Benzimidic acid ethyl is used as a chemical building block for the synthesis of a variety of pharmaceutical compounds, due to its potential biological activities and interest to researchers in the biomedical and pharmaceutical industries.
Used in Antimicrobial Applications:
Benzimidic acid ethyl is used as an antimicrobial agent for its potential to combat various types of infections caused by bacteria and other microorganisms.
Used in Antiviral Applications:
Benzimidic acid ethyl is used as an antiviral agent for its potential to inhibit the replication and spread of viruses.
Used in Anti-Inflammatory Applications:
Benzimidic acid ethyl is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Cancer Treatment:
Benzimidic acid ethyl is used as a potential therapeutic agent for treating various types of cancer, due to its potential biological activities and interest in drug development.
Used in Diabetes Treatment:
Benzimidic acid ethyl is used as a potential therapeutic agent for treating diabetes, due to its potential biological activities and interest in drug development.
Used in Cardiovascular Disease Treatment:
Benzimidic acid ethyl is used as a potential therapeutic agent for treating cardiovascular diseases, due to its potential biological activities and interest in drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 825-60-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 825-60:
(5*8)+(4*2)+(3*5)+(2*6)+(1*0)=75
75 % 10 = 5
So 825-60-5 is a valid CAS Registry Number.
825-60-5Relevant articles and documents
Preparation and ring transformation of isomeric β-lactam derivatives of bicyclic 1,3-thiazines
Fodor, Lajos,Csomós, Péter,Fül?p, Ferenc,Csámpai, Antal,Sohár, Pál
, p. 410 - 417 (2013)
Ketene-imine cycloaddition reactions between cis- and trans-2-aryl-4a,5,6, 7,8,8a-hexahydro-4H-3,1-benzothazines and chloroacetyl chloride in the presence of base were investigated. Because of the diastereotopic CN faces of cyclohexane-condensed thiazines
Sequential C-H activation enabled expedient delivery of polyfunctional arenes
Cai, Xiaoqing,Chen, Qian,Chen, Xiaojian,Gao, Yang,Huo, Yanping,Li, Xianwei,Ouyang, Wensen,Rao, Jianhang,Wang, Jie
supporting information, p. 8075 - 8078 (2021/08/20)
Modular construction of polyfunctional arenes from abundant feedstocks stands as an unremitting pursue in synthetic chemistry, accelerating the discovery of drugs and materials. Herein, using the multiple C-H activation strategy with versatile imidate esters, the expedient delivery of molecular libraries of densely functionalized sulfur-containing arenes was achieved, which enabled the concise construction of biologically active molecules, such as Bipenamol.
Synthesis of Highly Fused Pyrano[2,3- b]pyridines via Rh(III)-Catalyzed C-H Activation and Intramolecular Cascade Annulation under Room Temperature
Han, Xu,Gao, Feng,Li, Chunpu,Fang, Daqing,Xie, Xiong,Zhou, Yu,Liu, Hong
supporting information, p. 6281 - 6294 (2020/03/05)
A facile access to the polycyclic-fused pyrano[2,3-b]pyridines has been established under room temperature via Rh(III)-catalyzed C-H bond activation and intramolecular cascade annulation. This strategy features high efficiency, unique versatility, and gen
