4-Iodo-1-methyl-1H-imidazole-5-carbaldehyde

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Reagent Code: #47772
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CAS Number 189014-13-9

science Other reagents with same CAS 189014-13-9

blur_circular Chemical Specifications

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Weight 236.0105 g/mol
Formula C₅H₅IN₂O
badge Registry Numbers
MDL Number MFCD01632219
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is particularly valuable in the development of pharmaceuticals and bioactive compounds, where its structure allows for further functionalization. The iodine atom in the molecule serves as a reactive site for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. Additionally, the aldehyde group can undergo various transformations, including reductions, oxidations, or condensations, making it a key building block in medicinal chemistry. Its applications extend to the synthesis of imidazole-based drugs, which are often used in antifungal, antibacterial, and anticancer therapies. Researchers also explore its use in materials science for designing functional polymers or ligands in coordination chemistry.

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inventory 100mg
10-20 days ฿4,527.00

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4-Iodo-1-methyl-1H-imidazole-5-carbaldehyde
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is particularly valuable in the development of pharmaceuticals and bioactive compounds, where its structure allows for further functionalization. The iodine atom in the molecule serves as a reactive site for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. Additionally, the aldehyde group can undergo various

This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is particularly valuable in the development of pharmaceuticals and bioactive compounds, where its structure allows for further functionalization. The iodine atom in the molecule serves as a reactive site for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. Additionally, the aldehyde group can undergo various transformations, including reductions, oxidations, or condensations, making it a key building block in medicinal chemistry. Its applications extend to the synthesis of imidazole-based drugs, which are often used in antifungal, antibacterial, and anticancer therapies. Researchers also explore its use in materials science for designing functional polymers or ligands in coordination chemistry.

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