35681-66-4 Usage
Uses
Used in Pharmaceutical Industry:
1-Ethyl-5-iodo-2-methyl-4-nitro-1H-imidazole is used as an antimicrobial agent for its ability to combat various microorganisms, making it a potential candidate for the development of new antibiotics or antifungal drugs.
1-Ethyl-5-iodo-2-methyl-4-nitro-1H-imidazole is also used as an anti-inflammatory agent due to its capacity to reduce inflammation, which can be beneficial in the treatment of various inflammatory conditions.
Used in Agrochemical Industry:
1-Ethyl-5-iodo-2-methyl-4-nitro-1H-imidazole is used as a biocidal agent in agrochemicals for its potential to control pests and diseases in crops, thereby enhancing agricultural productivity.
Used in Materials Science:
1-Ethyl-5-iodo-2-methyl-4-nitro-1H-imidazole is used as a precursor in the synthesis of other organic compounds with potential applications in materials science, such as the development of new polymers or coatings with specific properties.
Used in Organic Electronics:
1-Ethyl-5-iodo-2-methyl-4-nitro-1H-imidazole is used as a component in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) or organic solar cells, due to its unique structure and properties that can contribute to improved device performance.
Check Digit Verification of cas no
The CAS Registry Mumber 35681-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,8 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35681-66:
(7*3)+(6*5)+(5*6)+(4*8)+(3*1)+(2*6)+(1*6)=134
134 % 10 = 4
So 35681-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H8IN3O2/c1-3-9-4(2)8-6(5(9)7)10(11)12/h3H2,1-2H3
35681-66-4Relevant academic research and scientific papers
Electrophilic iodination of 4-nitroimidazoles - A new high yielding method for the synthesis of 4-nitro-5-iodoimidazoles
Rao,Rao,Singh
, p. 353 - 366 (2007/10/02)
Electrophilic iodination of 4-nitroimidazoles employing the system KI- HNO3-AcOH provided a new route for the synthesis of 4-nitro-5-iodoimidazoles in high yields. With 2-unsubstituted-4-nitroimidazoles, 2,5-diiodo-4- nitroimidazoles were obtained.
