(S)-Benzyl 2-(8-amino-1-bromoimidazo[1,5-a]pyrazin-3-yl)pyrrolidine-1-carboxylate
97%
- Product Code: 71111
CAS:
1420478-88-1
| Molecular Weight: | 416.27 g./mol | Molecular Formula: | C₁₈H₁₈BrN₅O₂ |
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| EC Number: | MDL Number: | MFCD30184899 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring an imidazopyrazine core, makes it valuable for designing inhibitors or modulators used in treating diseases such as cancer, inflammation, or neurological disorders. Researchers often employ it in the preparation of novel therapeutic agents due to its potential to enhance selectivity and efficacy in drug candidates. Additionally, its bromo and amino functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,149.00 |
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| 0.250 | 10-20 days | ฿6,219.00 |
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| 1.000 | 10-20 days | ฿10,494.00 |
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(S)-Benzyl 2-(8-amino-1-bromoimidazo[1,5-a]pyrazin-3-yl)pyrrolidine-1-carboxylate
This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring an imidazopyrazine core, makes it valuable for designing inhibitors or modulators used in treating diseases such as cancer, inflammation, or neurological disorders. Researchers often employ it in the preparation of novel therapeutic agents due to its potential to enhance selectivity and efficacy in drug candidates. Additionally, its bromo and amino functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship (SAR) studies.
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