tert-Butyl 3-(((trifluoromethyl)sulfonyl)oxy)-2,5-dihydro-1H-pyrrole-1-carboxylate
98%
- Product Code: 44464
CAS:
630121-86-7
| Molecular Weight: | 317.2800 g./mol | Molecular Formula: | C₁₀H₁₄F₃NO₅S |
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| EC Number: | MDL Number: | MFCD23135802 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate for the construction of complex molecules. It is particularly valuable in the preparation of pyrrole derivatives, which are important in the development of pharmaceuticals, agrochemicals, and materials science. The trifluoromethylsulfonyloxy group (triflate) serves as an excellent leaving group, facilitating various substitution reactions, including cross-coupling reactions like Suzuki, Heck, and Sonogashira couplings. Its tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes and can be easily removed under mild acidic conditions, making it a useful tool in multi-step synthesis. This compound is also employed in the synthesis of biologically active compounds, including inhibitors and ligands for drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £99.33 |
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tert-Butyl 3-(((trifluoromethyl)sulfonyl)oxy)-2,5-dihydro-1H-pyrrole-1-carboxylate
This chemical is primarily used in organic synthesis as a versatile intermediate for the construction of complex molecules. It is particularly valuable in the preparation of pyrrole derivatives, which are important in the development of pharmaceuticals, agrochemicals, and materials science. The trifluoromethylsulfonyloxy group (triflate) serves as an excellent leaving group, facilitating various substitution reactions, including cross-coupling reactions like Suzuki, Heck, and Sonogashira couplings. Its tert-butyloxycarbonyl (Boc) protecting group ensures stability during synthetic processes and can be easily removed under mild acidic conditions, making it a useful tool in multi-step synthesis. This compound is also employed in the synthesis of biologically active compounds, including inhibitors and ligands for drug discovery programs.
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