tert-Butyl 3-iodo-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate
98%
- Product Code: 118219
CAS:
657428-43-8
| Molecular Weight: | 335.14 g./mol | Molecular Formula: | C₁₀H₁₄IN₃O₂ |
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| EC Number: | MDL Number: | MFCD28404922 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly as a versatile intermediate in the development of pharmaceutical compounds. Its structure, featuring both an iodo group and a protected amine, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions enable the creation of complex molecules, often targeting biologically active compounds or drug candidates. Additionally, the tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating the synthesis of pyrrolopyrazole derivatives, which are common scaffolds in medicinal chemistry. Its applications are particularly relevant in the design of kinase inhibitors and other therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿17,136.00 |
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| 0.250 | 10-20 days | ฿28,665.00 |
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tert-Butyl 3-iodo-2,6-dihydropyrrolo[3,4-c]pyrazole-5(4H)-carboxylate
This chemical is primarily utilized in organic synthesis, particularly as a versatile intermediate in the development of pharmaceutical compounds. Its structure, featuring both an iodo group and a protected amine, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions enable the creation of complex molecules, often targeting biologically active compounds or drug candidates. Additionally, the tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating the synthesis of pyrrolopyrazole derivatives, which are common scaffolds in medicinal chemistry. Its applications are particularly relevant in the design of kinase inhibitors and other therapeutic agents.
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