4-Iodo-2-methyl-5-nitro-1H-imidazole

95%

Reagent Code: #47780
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CAS Number 13369-83-0

science Other reagents with same CAS 13369-83-0

blur_circular Chemical Specifications

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Weight 253.0000 g/mol
Formula C₄H₄IN₃O₂
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MDL Number MFCD00210162
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description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring an imidazole ring with iodine, methyl, and nitro substituents, makes it a versatile building block for developing drugs with potential antimicrobial and antiparasitic properties. Researchers often employ it in the creation of compounds targeting protozoan infections, such as those caused by Trypanosoma and Leishmania species. Additionally, its reactive sites allow for further functionalization, enabling the development of novel therapeutic molecules with enhanced efficacy and specificity.

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inventory 250mg
10-20 days ฿1,503.00

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4-Iodo-2-methyl-5-nitro-1H-imidazole
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring an imidazole ring with iodine, methyl, and nitro substituents, makes it a versatile building block for developing drugs with potential antimicrobial and antiparasitic properties. Researchers often employ it in the creation of compounds targeting protozoan infections, such as those caused by Trypanosoma and Leishmania species. Additionall

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring an imidazole ring with iodine, methyl, and nitro substituents, makes it a versatile building block for developing drugs with potential antimicrobial and antiparasitic properties. Researchers often employ it in the creation of compounds targeting protozoan infections, such as those caused by Trypanosoma and Leishmania species. Additionally, its reactive sites allow for further functionalization, enabling the development of novel therapeutic molecules with enhanced efficacy and specificity.

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