3-(tert-Butyl)-1-iodoimidazo[1,5-a]pyrazin-8-amine
97%
- Product Code: 65075
CAS:
1320267-01-3
| Molecular Weight: | 316.14 g./mol | Molecular Formula: | C₁₀H₁₃IN₄ |
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| EC Number: | MDL Number: | MFCD20489128 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex heterocyclic compounds. Its structure makes it a valuable intermediate in the creation of pharmacologically active molecules, often serving as a building block in the synthesis of potential drug candidates. Researchers leverage its reactivity to introduce specific functional groups into target molecules, enabling the exploration of novel therapeutic agents. Additionally, it finds application in medicinal chemistry for the design and optimization of compounds targeting various biological pathways. Its unique properties also make it suitable for use in academic research, where it aids in the study of chemical reactions and mechanisms involving imidazo[1,5-a]pyrazine derivatives.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,260.01 |
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3-(tert-Butyl)-1-iodoimidazo[1,5-a]pyrazin-8-amine
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex heterocyclic compounds. Its structure makes it a valuable intermediate in the creation of pharmacologically active molecules, often serving as a building block in the synthesis of potential drug candidates. Researchers leverage its reactivity to introduce specific functional groups into target molecules, enabling the exploration of novel therapeutic agents. Additionally, it finds application in medicinal chemistry for the design and optimization of compounds targeting various biological pathways. Its unique properties also make it suitable for use in academic research, where it aids in the study of chemical reactions and mechanisms involving imidazo[1,5-a]pyrazine derivatives.
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