616234-82-3 Usage
Imidazole ring
A five-membered heterocyclic ring with three carbon atoms and two nitrogen atoms.
Phenyl groups
Two phenyl groups are present in the compound, contributing to its aromatic nature.
Propenyl group
A reactive alkenyl group (C3H5) is included in the molecular structure.
Phenylmethoxy group
A potential bioactive group (OCH2Ph) attached to the molecule, which could be relevant for drug development or other applications.
Aromatic character
The compound is highly aromatic due to the presence of multiple phenyl groups and the imidazole ring.
Reactivity
The compound may exhibit reactivity because of the propenyl group and the presence of the phenylmethoxy group.
Potential drug development
The presence of the phenyl group suggests the possibility of the compound interacting with biological targets, indicating potential for drug development or bioactive applications.
Need for further research
More studies are required to fully understand the properties and potential uses of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 616234-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,6,2,3 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 616234-82:
(8*6)+(7*1)+(6*6)+(5*2)+(4*3)+(3*4)+(2*8)+(1*2)=143
143 % 10 = 3
So 616234-82-3 is a valid CAS Registry Number.
616234-82-3Relevant academic research and scientific papers
Synthesis of fused tetrazole- and imidazole derivatives via iodocyclization
Ek, Fredrik,Wistrand, Lars-G?ran,Frejd, Torbj?rn
, p. 6759 - 6769 (2007/10/03)
The possibility to prepare fused tetrazole- and imidazole derivatives by iodocyclization in moderate to excellent yields is demonstrated. In some examples the cyclizations were not following Baldwin's rules entirely, i.e. exo-selectivity. Nucleophilic substitution of the formed iodides gave different results depending on the hardness of the nucleophile. Thus, elimination of the iodide could be a problem but a substitution reaction with ethyl potassium xanthate and a radical reaction using acrylonitrile were tolerated. In addition, we showed that it is possible to selectively use three iodo substituents individually in one of the fused imidazole derivatives.
