1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine
98%
- Product Code: 81753
CAS:
207857-15-6
| Molecular Weight: | 391.36 g./mol | Molecular Formula: | C₁₂H₂₀F₃N₃O₆S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 113°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized as a versatile reagent in organic synthesis, particularly in the preparation of protected guanidine derivatives. Its trifluoromethylsulfonyl group acts as a strong activating agent, facilitating the introduction of guanidine moieties into various organic molecules. This makes it valuable in the synthesis of pharmaceuticals, where guanidine structures are often key components due to their biological activity. Additionally, the Boc (tert-butoxycarbonyl) protecting groups provide stability and selectivity during multi-step synthetic processes, allowing for controlled reactions and easy deprotection when needed. Its application extends to the development of peptides, peptidomimetics, and other biologically active compounds, where precise functional group manipulation is essential.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| MELTING POINT | 113 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $44.20 |
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| 1.000 | 10-20 days | $99.45 |
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| 5.000 | 10-20 days | $426.42 |
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1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine
This chemical is primarily utilized as a versatile reagent in organic synthesis, particularly in the preparation of protected guanidine derivatives. Its trifluoromethylsulfonyl group acts as a strong activating agent, facilitating the introduction of guanidine moieties into various organic molecules. This makes it valuable in the synthesis of pharmaceuticals, where guanidine structures are often key components due to their biological activity. Additionally, the Boc (tert-butoxycarbonyl) protecting groups provide stability and selectivity during multi-step synthetic processes, allowing for controlled reactions and easy deprotection when needed. Its application extends to the development of peptides, peptidomimetics, and other biologically active compounds, where precise functional group manipulation is essential.
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