tert-Butyl (6-amino-7-iodo-1-methyl-1H-imidazo[4,5-c]pyridin-4-yl)(methyl)carbamate

95%

Reagent Code: #37100
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CAS Number 914942-88-4

science Other reagents with same CAS 914942-88-4

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Weight 403.2188 g/mol
Formula C₁₃H₁₈IN₅O₂
badge Registry Numbers
MDL Number MFCD29058807
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This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex molecules, particularly those targeting kinase inhibition. Its structure is often incorporated into the development of potential therapeutic agents for treating various diseases, including cancer and inflammatory conditions. The iodine atom in the molecule allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for biological evaluation. Researchers leverage its unique imidazo[4,5-c]pyridine core to design compounds with enhanced selectivity and potency against specific biological targets.

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inventory 100mg
10-20 days ฿23,004.00

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tert-Butyl (6-amino-7-iodo-1-methyl-1H-imidazo[4,5-c]pyridin-4-yl)(methyl)carbamate
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This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex molecules, particularly those targeting kinase inhibition. Its structure is often incorporated into the development of potential therapeutic agents for treating various diseases, including cancer and inflammatory conditions. The iodine atom in the molecule allows for further functionalization through cross-coupling reactions, enabling the creatio

This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex molecules, particularly those targeting kinase inhibition. Its structure is often incorporated into the development of potential therapeutic agents for treating various diseases, including cancer and inflammatory conditions. The iodine atom in the molecule allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for biological evaluation. Researchers leverage its unique imidazo[4,5-c]pyridine core to design compounds with enhanced selectivity and potency against specific biological targets.

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