3575-07-3 Usage
Description
2,2'-ethane-1,2-diylbis-1H-benzimidazole, also known as EDBI, is a chemical compound belonging to the benzimidazole class. It is recognized for its high selectivity and sensitivity as a fluorescent probe, particularly for the detection of metal ions such as zinc ions. EDBI's potential extends to various applications in biological and medical fields, including drug delivery and imaging techniques for cancer detection, as well as antimicrobial and antiviral properties, making it a versatile compound for research and industry.
Uses
Used in Research Applications:
2,2'-ethane-1,2-diylbis-1H-benzimidazole is used as a fluorescent probe for the detection of metal ions, particularly zinc ions, due to its high selectivity and sensitivity.
Used in Biological and Medical Fields:
2,2'-ethane-1,2-diylbis-1H-benzimidazole is used as a potential drug delivery agent and in imaging techniques for cancer detection, leveraging its properties for enhanced diagnostic and therapeutic approaches.
Used in Antimicrobial and Antiviral Applications:
2,2'-ethane-1,2-diylbis-1H-benzimidazole is utilized for its antimicrobial and antiviral properties, indicating its potential in combating infections and diseases.
Used in Industry:
2,2'-ethane-1,2-diylbis-1H-benzimidazole is employed in various industrial applications, capitalizing on its versatility and diverse potential uses in research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 3575-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3575-07:
(6*3)+(5*5)+(4*7)+(3*5)+(2*0)+(1*7)=93
93 % 10 = 3
So 3575-07-3 is a valid CAS Registry Number.
3575-07-3Relevant articles and documents
Boric acid-catalyzed direct condensation of carboxylic acids with benzene-1,2-diamine into benzimidazoles
Maras, Nenad,Kocevar, Marijan
experimental part, p. 1860 - 1874 (2011/12/02)
The applicability of boric acid catalysis for the direct condensation of carboxylic acids with benzene-1,2-diamine to give 2-substituted benzimidazoles was investigated. It was found that catalytic amounts (5-10 mol-%) of boric acid efficiently promote the cyclocondensation of aliphatic carboxylic acids in refluxing toluene. In addition, the relatively neutral conditions allow the use of acid-sensitive substrates and give rise to specific transformations and selectivities that are not observed with some classical methods. Benzoic acids were found to be less reactive than aliphatic acids and thus require refluxing xylene for better efficiency. Phenylboronic acid was found to be inactive as a catalyst due to its rapid consumption by condensation with benzene-1,2-diamine to give a 2-phenylbenzodiazaborole. Copyright