tert-Butyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-5(1H,4H,6H)-carboxylate
97%
- Product Code: 83619
CAS:
398491-61-7
| Molecular Weight: | 252.31 g./mol | Molecular Formula: | C₁₂H₂₀N₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275051 | |
| Melting Point: | Boiling Point: | 420.6°C | |
| Density: | 1.207 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the development of pharmaceutical compounds. Its structure is well-suited for constructing complex heterocyclic frameworks, which are often found in biologically active molecules. It is commonly employed in the synthesis of potential drug candidates targeting various therapeutic areas, including central nervous system disorders and cancer. Researchers also leverage its reactivity to introduce functional groups or modify existing structures, enabling the exploration of structure-activity relationships in drug discovery. Additionally, its stability and compatibility with various reaction conditions make it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft4,525.13 |
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| 1.000 | 10-20 days | Ft16,699.87 |
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tert-Butyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-5(1H,4H,6H)-carboxylate
This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the development of pharmaceutical compounds. Its structure is well-suited for constructing complex heterocyclic frameworks, which are often found in biologically active molecules. It is commonly employed in the synthesis of potential drug candidates targeting various therapeutic areas, including central nervous system disorders and cancer. Researchers also leverage its reactivity to introduce functional groups or modify existing structures, enabling the exploration of structure-activity relationships in drug discovery. Additionally, its stability and compatibility with various reaction conditions make it a versatile building block in medicinal chemistry.
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