201299-82-3 Usage
Derivative of benzimidazole
Benzimidazole is a heterocyclic compound that contains a benzene ring fused to an imidazole ring This indicates that the compound has a complex ring structure with various potential chemical interactions.
Presence of propenyl group
A straight chain, three-carbon compound with a double bond This suggests that the compound has a specific functional group that can participate in chemical reactions and contribute to its potential applications.
Potential applications in pharmaceuticals
Benzimidazole derivatives exhibit a wide range of pharmacological activities This suggests that 1H-Benzimidazol-2-amine, 1-(2-propenyl)-(9CI) could have possible uses in the development of new drugs.
Pharmacological activities
Antimicrobial, antiviral, and anticancer properties These activities indicate that the compound may have therapeutic potential in treating various diseases and conditions.
Need for further research
To explore the potential uses and effects of 1H-Benzimidazol-2-amine, 1-(2-propenyl)-(9CI) in various fields This highlights the importance of continued investigation into the properties and applications of 1H-Benzimidazol-2-amine,1-(2-propenyl)-(9CI).
Check Digit Verification of cas no
The CAS Registry Mumber 201299-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,2,9 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 201299-82:
(8*2)+(7*0)+(6*1)+(5*2)+(4*9)+(3*9)+(2*8)+(1*2)=113
113 % 10 = 3
So 201299-82-3 is a valid CAS Registry Number.
201299-82-3Relevant articles and documents
Imidazo[1,2-a]benzimidazole derivatives: XXVIII. Syntheses and heterocyclizations on the basis of 1-allyl-2-aminobenzimidazole
Anisimova,Tolpygin
experimental part, p. 1346 - 1353 (2011/12/05)
Addition of hydrogen bromide at the double bond of 1-allyl-2-amino-1H- benzimidazole and 3-alkyl-(benzyl)-1-allyl-2-amino-1H-benzimidazolium halides was studied. The resulting 1-(2-bromopropyl) derivatives were subjected to thermolysis under different conditions, and the structure of dehydrobromination products was determined and proved by independent synthesis via prototropic isomerization of the allyl group by the action of bases. Pleiades Publishing, Ltd., 2011.
Synthesis and?QSAR studies of?novel 1-substituted-2-aminobenzimidazoles derivatives
Guida, Xuan,Jianhua, Han,Xiaomin, Li
, p. 1080 - 1083 (2007/10/03)
A series of novel 1-substituted-2-aminobenzimidazole derivatives were synthesized. The structures of the synthesized compounds were confirmed by 1H-NMR spectra and by elemental analysis. Acute toxicities of these compounds were detected on mice via toxicity (logLD50). QSAR analysis of these chemicals was studied on the relationship between acute toxicity and the octanol/water partition coefficient (LogP). The products were identified by the results of elemental analysis and 1H-NMR spectra. The toxicity (logLD50) of 2-aminobenzimidazole 1-substituents were correlated well with the partition coefficient LogP, r = 0.9243. The bioactivity (toxicity) of 2-aminobenzimidazoles can be predicted by the molecular structural parameter such as LogP.
