7-Bromo-6-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole
≥95%
- Product Code: 52446
CAS:
1956386-57-4
| Molecular Weight: | 341.32 g./mol | Molecular Formula: | C₁₄H₂₁BrN₂OSi |
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| Density: | Storage Condition: | Room temperature, dry and sealed |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $334.47 |
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| 0.250 | 10-20 days | $668.94 |
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7-Bromo-6-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole
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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