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
Understanding Mechanochromic Luminescence on Account of Molecular Level Based on Phosphorescent Iridium(III) Complex Isomers
Li, Guangfu,Yang, Tianzhi,Shao, Kuizhan,Gao, Ying,Shan, Guogang,Su, Zhongmin,Wang, Xinlong,Zhu, Dongxia
, p. 3741 - 3748 (2021/04/07)
Mechanochromic luminescent (MCL) materials are promising in pressure sensors, security papers, photoelectric devices and optical data recording. Although some kinds of MCL-active iridium(III) complexes with various soft substituent functional ligands (e.g
An efficient, stereocontrolled and versatile synthetic route to bicyclic partially saturated privileged scaffolds
Bond, Andrew D.,Hanby, Abigail R.,King, Thomas A.,Moss, Thomas A.,Sore, Hannah F.,Spring, David R.,Stewart, Hannah L.
supporting information, p. 6818 - 6821 (2020/07/04)
Herein, we describe the development of a simple, high yielding and stereocontrolled strategy for the synthesis of a series of triazolopiperazines and other biologically relevant fused scaffolds from optically active amino acids. This route was applied to the synthesis of 22 scaffolds containing new, previously inaccessible vectors and used to access a novel analogue of ganaplacide.
