5-Bromo-3-Iodo-1-((2-(Trimethylsilyl)Ethoxy)Methyl)-1H-Indazole

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Reagent Code: #153950
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CAS Number 918440-14-9

science Other reagents with same CAS 918440-14-9

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Weight 453.19 g/mol
Formula C₁₃H₁₈BrIN₂OSi
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. The 1-((2-(Trimethylsilyl)ethoxy)methyl) (SEM) group acts as a stable protecting group for the indazole nitrogen, removable under mild acidic conditions for precise multi-step synthesis control. Its functional groups, including bromine at the 5-position and iodine at the 3-position, enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to design potent and selective bioactive molecules, especially in targeted therapies. Also utilized in the preparation of radiolabeled analogs for imaging studies due to the presence of bromine and iodine atoms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,160.00
inventory 250mg
10-20 days ฿41,930.00

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5-Bromo-3-Iodo-1-((2-(Trimethylsilyl)Ethoxy)Methyl)-1H-Indazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. The 1-((2-(Trimethylsilyl)ethoxy)methyl) (SEM) group acts as a stable protecting group for the indazole nitrogen, removable under mild acidic conditions for precise multi-step synthesis control. Its functional groups, including bromine at the 5-position and iodine at the 3-position, enable selective cross-coupling reactions, making it valuable in medicinal ch

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. The 1-((2-(Trimethylsilyl)ethoxy)methyl) (SEM) group acts as a stable protecting group for the indazole nitrogen, removable under mild acidic conditions for precise multi-step synthesis control. Its functional groups, including bromine at the 5-position and iodine at the 3-position, enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to design potent and selective bioactive molecules, especially in targeted therapies. Also utilized in the preparation of radiolabeled analogs for imaging studies due to the presence of bromine and iodine atoms.

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