5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1H-indazole
95%
- Product Code: 87554
CAS:
1254473-76-1
| Molecular Weight: | 374.29 g./mol | Molecular Formula: | C₁₃H₁₉IN₂OSi |
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| EC Number: | MDL Number: | MFCD26096717 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used in organic synthesis as a versatile intermediate, particularly in the development of pharmaceutical compounds. Its structure, featuring both a silyl-protected hydroxyl group and an iodine atom, allows for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce indazole derivatives into target structures. Additionally, it serves as a precursor in the synthesis of biologically active molecules, including potential drug candidates targeting various diseases. The tert-butyldimethylsilyl group provides stability during reactions, while the iodine atom acts as a reactive site for further modifications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $384.64 |
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| 0.250 | 10-20 days | $714.32 |
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| 1.000 | 10-20 days | $1,428.64 |
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5-((tert-Butyldimethylsilyl)oxy)-3-iodo-1H-indazole
Used in organic synthesis as a versatile intermediate, particularly in the development of pharmaceutical compounds. Its structure, featuring both a silyl-protected hydroxyl group and an iodine atom, allows for selective functionalization, making it valuable in constructing complex molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce indazole derivatives into target structures. Additionally, it serves as a precursor in the synthesis of biologically active molecules, including potential drug candidates targeting various diseases. The tert-butyldimethylsilyl group provides stability during reactions, while the iodine atom acts as a reactive site for further modifications.
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