7-Bromo-6-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole

≥95%

Reagent Code: #52446
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CAS Number 1956386-57-4

science Other reagents with same CAS 1956386-57-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.32 g/mol
Formula C₁₄H₂₁BrN₂OSi
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, especially those targeting specific enzymes or receptors. The presence of the trimethylsilyl ethoxymethyl (SEM) group makes it a valuable protecting group for nitrogen atoms during complex multi-step reactions, ensuring selective transformations. Additionally, its indazole core structure is often explored in medicinal chemistry for designing potential drug candidates, particularly in areas such as oncology, inflammation, and central nervous system disorders. Its bromo and methyl substituents further enhance its reactivity, enabling precise modifications to create diverse derivatives for biological evaluation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,505.00
inventory 250mg
10-20 days ฿17,010.00

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7-Bromo-6-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, especially those targeting specific enzymes or receptors. The presence of the trimethylsilyl ethoxymethyl (SEM) group makes it a valuable protecting group for nitrogen atoms during complex multi-step reactions, ensuring selective transformations. Additionally, its indazole core structu

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, especially those targeting specific enzymes or receptors. The presence of the trimethylsilyl ethoxymethyl (SEM) group makes it a valuable protecting group for nitrogen atoms during complex multi-step reactions, ensuring selective transformations. Additionally, its indazole core structure is often explored in medicinal chemistry for designing potential drug candidates, particularly in areas such as oncology, inflammation, and central nervous system disorders. Its bromo and methyl substituents further enhance its reactivity, enabling precise modifications to create diverse derivatives for biological evaluation.

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