59918-84-2 Usage
Uses
Used in Medicinal Chemistry:
2-(selenophen-2-yl)-1H-benzimidazole is used as a compound of interest for its potential pharmaceutical applications. The presence of selenium, a trace element known for its antioxidant properties, may contribute to the development of new drugs with enhanced therapeutic effects.
Used in Material Science:
In the field of material science, 2-(selenophen-2-yl)-1H-benzimidazole is used as a compound with potential for the development of new materials. Its unique structure and properties could be harnessed to create innovative materials with specific characteristics for various applications.
Used in Antioxidant Applications:
2-(selenophen-2-yl)-1H-benzimidazole is used as an antioxidant agent, leveraging the antioxidant properties of selenium to protect cells from oxidative stress and potentially reduce the risk of certain diseases.
Used in Drug Delivery Systems:
2-(selenophen-2-yl)-1H-benzimidazole is used as a component in drug delivery systems, where its unique structure may improve the delivery, bioavailability, and therapeutic outcomes of various pharmaceuticals.
Used in Industrial Applications:
2-(selenophen-2-yl)-1H-benzimidazole is used in industrial applications, where its specific properties may be utilized in the development of new products or processes, such as in the production of specialty chemicals or materials with unique characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 59918-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,1 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59918-84:
(7*5)+(6*9)+(5*9)+(4*1)+(3*8)+(2*8)+(1*4)=182
182 % 10 = 2
So 59918-84-2 is a valid CAS Registry Number.
59918-84-2Relevant academic research and scientific papers
El'chaninov, M. M.,Magdesieva, N. N.,Simonov, A. M.,Chovnikova, N. G.
, p. 1216 - 1219 (1983)
2-(2'-Selenienyl)benzimidazole has been synthesized by a Weidenhagen reaction and converted into the N-methylated derivative.Electrophilic-substitution reactions (nitration, sulfonation, bromination, chloromethylation, and acylation) in the selenophene ri
