10045-66-6 Usage
General Description
4,5-diiodo-2-phenyl-1H-imidazole is a chemical compound with the molecular formula C9H6I2N2. It is a derivative of imidazole and contains two iodine atoms and a phenyl group. 4,5-diiodo-2-phenyl-1H-imidazole is commonly used in organic synthesis and pharmaceutical research due to its potential biological activities. It has been studied for its antifungal, antibacterial, and antiparasitic properties, and also shows promise for use in photodynamic therapy for cancer treatment. Additionally, 4,5-diiodo-2-phenyl-1H-imidazole has been investigated for its potential as a corrosion inhibitor and as a precursor in the production of other heterocyclic compounds. Overall, this chemical compound has a variety of potential applications in the fields of medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 10045-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,4 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10045-66:
(7*1)+(6*0)+(5*0)+(4*4)+(3*5)+(2*6)+(1*6)=56
56 % 10 = 6
So 10045-66-6 is a valid CAS Registry Number.
10045-66-6Relevant articles and documents
Aromatic iodination in aqueous solution. A new lease of life for aqueous potassium dichloroiodate
Garden, Simon J.,Torres, José C.,De Souza Melo, Simone C.,Lima, Alexandre S.,Pinto, Angelo C.,Lima, Edson L.S.
, p. 2089 - 2092 (2001)
A re-investigation of the use of aqueous potassium dichloroiodate (KICl2) as an iodinating agent for aromatic compounds has found the reagent to be more generally applicable than previously known. The reagent has been found to give excellent yields of iodinated heterocyclic compounds, such as isatin, imidazole and pyrazole.
A Pd-catalyzed double coupling reaction to 4,5-disubstituted imidazole alkynes
Kim,Kang,Ryu,Keum,Seo
, p. 507 - 512 (2007/10/03)
A palladium-catalyzed double coupling reaction of 4,5-diiodoimidazoles 2, which were prepared by diiodination of imidazole, and terminal alkynes provided the corresponding imidazole diynes 3.
