7256-17-9 Usage
Molecular Structure
The compound is a pentitol derivative that contains a benzimidazole moiety. This means it is a sugar alcohol (pentitol) that has been modified to include a benzimidazole group.
Potential Biological Activity
The compound has potential biological activity, meaning it could interact with biological systems and potentially have therapeutic effects.
Benzimidazole Derivative
The presence of the benzimidazole group is significant. Benzimidazole derivatives are known for their antifungal, antibacterial, and antiviral properties, and are often researched for their potential use in pharmaceuticals.
Chlorine Substitution
The compound includes a chlorine atom at the 6-position of the benzimidazole ring. This could affect the compound's reactivity, stability, and interaction with biological systems.
Potential Applications
Given its structure and the properties of similar compounds, 1-C-(6-chloro-1H-benzimidazol-2-yl)pentitol may have applications in the development of new drugs or treatments for various diseases and conditions.
Need for Further Research
While the compound shows promise, further research and studies are needed to fully understand and harness its potential. This includes testing for efficacy, safety, and potential side effects in various biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 7256-17-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7256-17:
(6*7)+(5*2)+(4*5)+(3*6)+(2*1)+(1*7)=99
99 % 10 = 9
So 7256-17-9 is a valid CAS Registry Number.
7256-17-9Relevant articles and documents
Studies on saccharide benzimidazoles: 2-(β-D-gulofuranosyl)benzimidazole and 2-(β-D-glucofuranosyl)benzimidazole C-nucleoside analogs; synthesis, anomeric configuration and antifouling potency
Labib, Gorgina M. H.,Matsuo, Koichi,Salem, Dalia M. S. A.,Sallam, Mohammed A. E.,Youssef, Trevena N. M. A.
, (2020/08/19)
A series of acyclic 2-(D-gulo-) and 2-(D-gluco-)benzimidazole C-nucloside analogs have been prepared by condensation of o-phenylenediamine dihydrochloride derivatives with D-gulonic acid-γ-lactone and D-gluconic acid-γ-lactone, separately. Acid catalyzed dehydrative cyclization of the acyclic benzimidazole C-nucleoside afforded the corresponding 2-(β-D-gulo-) and 2-(β-D-gluco-)furanosyl benzimidazole C-nucleoside analogs. The structure and the anomeric configuration of C-nucleoside analogs obtained were determined by periodate oxidation, 1H NMR, UV and circular dichroism (CD) spectroscopy. The antifouling property of C-nucleoside analogs has been studied using antibacterial biofilm test. 2-(D-gulo-) and 2-(D-gluco-)benzimidazole analogs were useful for inhibiting marine bacterial growth and did not cause any bad effect to the surrounding seawater.
