1217102-00-5 Usage
Derivative of benzimidazole
Heterocyclic organic compound This compound is derived from benzimidazole, which is a heterocyclic organic compound containing a ring of carbon and nitrogen atoms.
Substitution pattern
Methyl groups at 2, 5, and 7 positions The benzimidazole ring has methyl groups attached to it at the 2nd, 5th, and 7th positions, which affects its chemical properties and potential applications.
Phenyl group
At the 1 position A phenyl group, a ring of six carbon atoms with delocalized electrons, is attached to the 1st position of the benzimidazole ring, further influencing the compound's properties.
Pharmacological activities
Antimicrobial, antiviral, anticancer, and anti-inflammatory Benzimidazoles, in general, are known for their wide range of pharmacological activities, which include fighting infections, viruses, cancer, and inflammation.
Potential applications
New pharmaceutical drugs and research tools Due to its unique structure and potential pharmacological properties, 2,5,7-trimethyl-1-phenyl-1H-benzimidazole may be useful in the development of new drugs or as a research tool in chemical and biological studies.
Check Digit Verification of cas no
The CAS Registry Mumber 1217102-00-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,1,0 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1217102-00:
(9*1)+(8*2)+(7*1)+(6*7)+(5*1)+(4*0)+(3*2)+(2*0)+(1*0)=85
85 % 10 = 5
So 1217102-00-5 is a valid CAS Registry Number.
1217102-00-5Relevant articles and documents
Reactivity-controlled regioselectivity: A regiospecific synthesis of 1,2-disubstituted benzimidazoles
Deng, Xiaohu,Mani, Neelakandha S.
experimental part, p. 680 - 686 (2010/03/04)
We demonstrate exceptional levels of regioselectivity in the tandem, animation reactions between 1,2-differentiated dihaloarenes and N-substituted amidines, The regiochemical outcome of this Cul-catalyzed reaction is achieved through a combination of N1/N2 chemoselectivity on the amidine and reactivity-controlled X1/X2 chemoselectivity on the 1,2-dihaloarene. This reaction proves to be fairly general for the regiospecific synthesis of 1,2-substituted benzimidazoles.
