3652-97-9 Usage
Benzimidazole derivative
The compound is derived from benzimidazole, which is a heterocyclic aromatic organic compound known for its chemical stability and various applications in pharmaceuticals, agrochemicals, and materials science.
Nitrophenyl group
The presence of a nitrophenyl group (-C6H4NO2) in the structure of the compound adds to its chemical reactivity and potential applications in different fields.
Scientific research applications
The compound is used in various scientific research fields, making it an important subject for further study and exploration.
Potential pharmaceutical applications
Due to its unique structure and properties, the compound may have potential uses in the development of new drugs and therapies.
Potential agrochemical applications
The compound may also be used in the development of new agrochemicals, such as pesticides and fertilizers, to improve crop yield and protect plants from pests and diseases.
Potential materials science applications
The compound's unique properties may contribute to the development of new materials with specific characteristics, such as high strength, lightweight, or resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 3652-97-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3652-97:
(6*3)+(5*6)+(4*5)+(3*2)+(2*9)+(1*7)=99
99 % 10 = 9
So 3652-97-9 is a valid CAS Registry Number.
3652-97-9Relevant academic research and scientific papers
Synthesis and Autoxidation of 1,3-Dialkyl-2-arylbenzimidazolines
Reddy, A. Pandu Ranga,Veeranagaiah, V.,Ratnam, C. V.
, p. 367 - 371 (2007/10/02)
During the attempted studies of the elimination reactions of 1,3-dimethyl-(I, R = CH3)- and 1,3-diethyl-(I, R = C2H5)-2-arylbenzimidazolines, a novel rearrangement has been observed to take place resulting in substituted amides by autoxidative ring-opening.
