616234-84-5 Usage
Heterocyclic aromatic compound
The chemical contains an imidazole ring, which is a five-membered ring with one nitrogen atom and four carbon atoms.
Imidazole ring
The core structure of the compound, consisting of a five-membered ring with one nitrogen atom and four carbon atoms.
2-Substituted imidazole
The imidazole ring is substituted at the 2-position with a specific functional group.
2-[2-(3-Methyl-3-buten-1-yl)phenyl] group
The substituent attached to the 2-position of the imidazole ring, which consists of a phenyl group with a 3-methyl-3-buten-1-yl group attached to it.
3-Methyl-3-buten-1-yl group
A functional group within the substituent, consisting of a 3-buten-1-yl group with a methyl group attached to the third carbon.
Biologically active compounds
Imidazoles are found in a variety of biologically active compounds, making them important building blocks in organic synthesis.
Potentially useful intermediate
The specific substitution pattern on the imidazole ring in this chemical makes it a potentially useful intermediate for the synthesis of pharmaceuticals or other organic compounds.
Unique structure and reactivity
The compound's structure and reactivity make it a valuable tool in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 616234-84-5 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 616234-84:
(8*6)+(7*1)+(6*6)+(5*2)+(4*3)+(3*4)+(2*8)+(1*4)=145
145 % 10 = 5
So 616234-84-5 is a valid CAS Registry Number.
616234-84-5Relevant 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.
