149510-85-0 Usage
Uses
Used in Organic Synthesis:
2,5-Diiodo-4-methylimidazole is utilized as a key building block in organic synthesis for the creation of a variety of biologically active molecules. Its unique structure allows for the development of new compounds with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,5-Diiodo-4-methylimidazole is employed as a precursor in the synthesis of pharmaceuticals. Its chemical properties make it a valuable component in the development of new drugs with diverse therapeutic potentials.
Used in Antimicrobial and Antifungal Drug Development:
2,5-Diiodo-4-methylimidazole is investigated for its potential antimicrobial and antifungal properties, making it a promising candidate for the development of new treatments in the medical field. Its ability to combat microbial infections positions it as a subject of interest for researchers seeking innovative solutions to antibiotic resistance and fungal infections.
Overall, 2,5-Diiodo-4-methylimidazole's versatility and potential applications across different sectors underscore its importance in the ongoing pursuit of advancements in chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 149510-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,5,1 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149510-85:
(8*1)+(7*4)+(6*9)+(5*5)+(4*1)+(3*0)+(2*8)+(1*5)=140
140 % 10 = 0
So 149510-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H4I2N2/c1-2-3(5)8-4(6)7-2/h1H3,(H,7,8)
149510-85-0Relevant articles and documents
Efficient Synthesis of tert-Butyl 2,4-Dialkynylated and 2-Alkynylated-4-Arylated-1H-Imidazole-1-Carboxylate via Regioselective Sonogashira Cross-Coupling Reaction
Jismy, Badr,El Qami, Abdelkarim,Jacquemin, Johan,Guillot, Regis,Tikad, Abdellatif,Abarbri, Mohamed
, p. 4495 - 4507 (2021)
An efficient regioselective cross-coupling reactions of tert-butyl 2,4-dibrominated-5-methyl-1H-imidazole-1-carboxylate is reported. This new synthetic route runs under simple and mild conditions and selectively gives an easy access to 2,4-dialkynylated a
HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS AND COMBINATIONS THEREOF
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Page/Page column 86; 87; 108, (2015/07/07)
Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by disregulation of a fatty acid synthase pathway by the administration of such compounds and combinations of such compounds and other therapeutic agents.
HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS
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Page/Page column 72; 93, (2014/01/18)
Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by disregulation of a fatty acid synthase pathway by the administration of such compounds.
