10252-95-6 Usage
Chemical Family
Benzimidazole
Explanation
Different sources of media describe the Explanation of 10252-95-6 differently. You can refer to the following data:
1. The compound belongs to the benzimidazole family, which is a group of organic compounds known for their various applications in pharmaceuticals, agrochemicals, and other industries.
2. The compound has a chlorine atom substituted at the 6th position of the benzimidazole ring, which can influence its chemical properties and potential applications.
3. Dihydro Pyrrolo Ring System
3. The compound features a dihydro pyrrolo ring system, which is a reduced form of the pyrrolo ring. This can affect the compound's reactivity, solubility, and other properties.
4. Potential Pharmacological Activities
4. 1H-Pyrrolo[1,2-a]benzimidazole,6-chloro-2,3-dihydro-(7CI,8CI,9CI) may exhibit pharmacological activities, making it a candidate for further research and development in the pharmaceutical industry.
5. Applications in Medicinal Chemistry
5. Due to its unique chemical structure and potential pharmacological activities, the compound may be suitable for applications in medicinal chemistry, such as the development of new drugs or drug delivery systems.
6. Drug Discovery
7. Further Research and Study Needed
6. To fully understand the potential uses and effects of 1H-Pyrrolo[1,2-a]benzimidazole,6-chloro-2,3-dihydro-(7CI,8CI,9CI), further research and study are required. This may include in vitro and in vivo testing, as well as investigation into its mechanism of action and potential side effects.
Chloro Substitution
6th position
Check Digit Verification of cas no
The CAS Registry Mumber 10252-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10252-95:
(7*1)+(6*0)+(5*2)+(4*5)+(3*2)+(2*9)+(1*5)=66
66 % 10 = 6
So 10252-95-6 is a valid CAS Registry Number.
10252-95-6Relevant articles and documents
Metal-Free Sequential C(sp2)-H/OH and C(sp3)-H Aminations of Nitrosoarenes and N-Heterocycles to Ring-Fused Imidazoles
Purkait, Anisha,Roy, Subhra Kanti,Srivastava, Hemant Kumar,Jana, Chandan K.
, p. 2540 - 2543 (2017)
Hydrogen bond assisted ortho-selective C(sp2)-H amination of nitrosoarenes and subsequent α-C(sp3)-H functionalization of aliphatic amines is achieved under metal-free conditions. The annulation of nitrosoarenes and 2-hydroxy-C-nitroso compounds with N-heterocycles provides a facile excess to a wide range of biologically relevant ring-fused benzimidazoles and structurally novel polycyclic imidazoles, respectively. Nucleophilic aromatic hydrogen substitution (SNArH) was found to be preferred over classical SNAr reaction during the C(sp2)-H amination of halogenated nitrosoarenes.
Functionalized orthoesters as powerful building blocks for the efficient preparation of heteroaromatic bicycles
Bastug, Gulluzar,Eviolitte, Christophe,Markó, István E.
, p. 3502 - 3505 (2012/08/08)
By combining substituted anilines with functionalized orthoesters, an efficient and connective methodology for the preparation of benzoxazole, benzothiazole, and benzimidazole derivatives has been established. The versatility of this approach enables the development of new libraries of heterocycles containing multifunctional sites.
