198127-92-3 Usage
Uses
Used in Organic Chemistry Research:
N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is used as a research compound for its unique chemical properties. Its complex structure makes it a valuable tool in the exploration of new chemical reactions and processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is used as a potential candidate for drug development. Its chemical composition may contribute to the creation of new medications, particularly in the areas of organic chemistry and medicinal chemistry.
Used in Material Science:
N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is employed as a component in the development of new materials. Its unique chemical structure may offer properties that can be harnessed in the creation of advanced materials with specific characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 198127-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,1,2 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 198127-92:
(8*1)+(7*9)+(6*8)+(5*1)+(4*2)+(3*7)+(2*9)+(1*2)=173
173 % 10 = 3
So 198127-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H7I2N3O2S/c1-9(2)13(11,12)10-3-8-4(6)5(10)7/h3H,1-2H3
198127-92-3Relevant academic research and scientific papers
Synthesis and Diels-Alder reactions of 4-vinylimidazoles
Lovely, Carl J.,Du, Hongwang,Dias, H. V. Rasika
, p. 1319 - 1322 (2007/10/03)
(equation presented) The synthesis of several 4-vinylimidazoles via Stille cross-coupling reactions of the corresponding protected 4-iodoimidazoles with tributylvinylstannane is described. These heterocyclic dienes are shown to be effective partners in th
Polyfunctionalisation of imidazole via sequential imidazolyl anion formation
Carver, David S.,Lindell, Stephen D.,Saville-Stones, Elizabeth A.
, p. 14481 - 14496 (2007/10/03)
A method for achieving the sequential functionalisation of the imidazole ring in the order C-5→C-4→C-2 is described. The chemistry proceeds via the regioselective formation of positionally stable imidazolyl anions which are reacted with electrophiles (aldehydes, alkyl halides, azides, formamides, isocyanates) to afford substituted imidazoles in 31-90% yield.
