5-(tert-Butoxycarbonyl)-4,5,6,7-tetrahydro-[1,2,3]triazolo[1,5-a]pyrazine-3-carboxylic acid
≥95%
- Product Code: 87567
CAS:
1251002-60-4
| Molecular Weight: | 268.27 g./mol | Molecular Formula: | C₁₁H₁₆N₄O₄ |
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| EC Number: | MDL Number: | MFCD14581554 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily used in the field of organic synthesis, particularly as a building block for the development of more complex molecules. It is often employed in the preparation of pharmaceutical intermediates, where its unique structure allows for the introduction of triazole and pyrazine moieties into target compounds. These features are valuable in drug discovery, especially for designing molecules with potential biological activity. The tert-butoxycarbonyl (Boc) protecting group in the compound is particularly useful in peptide synthesis, as it can be selectively removed under mild acidic conditions, allowing for controlled reactions. Additionally, its carboxylic acid functionality enables further derivatization, making it a versatile reagent in medicinal chemistry and materials science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿4,437.00 |
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| 0.005 | 10-20 days | ฿7,578.00 |
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5-(tert-Butoxycarbonyl)-4,5,6,7-tetrahydro-[1,2,3]triazolo[1,5-a]pyrazine-3-carboxylic acid
This compound is primarily used in the field of organic synthesis, particularly as a building block for the development of more complex molecules. It is often employed in the preparation of pharmaceutical intermediates, where its unique structure allows for the introduction of triazole and pyrazine moieties into target compounds. These features are valuable in drug discovery, especially for designing molecules with potential biological activity. The tert-butoxycarbonyl (Boc) protecting group in the compound is particularly useful in peptide synthesis, as it can be selectively removed under mild acidic conditions, allowing for controlled reactions. Additionally, its carboxylic acid functionality enables further derivatization, making it a versatile reagent in medicinal chemistry and materials science.
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