((1-(tert-Butoxycarbonyl)piperidin-4-yl)methyl)triphenylphosphonium iodide
≥95%
- Product Code: 36055
CAS:
146293-11-0
| Molecular Weight: | 587.47 g./mol | Molecular Formula: | C₂₉H₃₅INO₂P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20271861 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the synthesis of pharmaceuticals, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, ensuring selective reactions during multi-step processes. The triphenylphosphonium moiety makes it useful in Wittig reactions, which are employed to form alkenes from carbonyl compounds. This makes it valuable in the production of fine chemicals, agrochemicals, and bioactive compounds. Additionally, its structure allows for modifications in drug discovery, enabling the creation of novel compounds with potential therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,601.00 |
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((1-(tert-Butoxycarbonyl)piperidin-4-yl)methyl)triphenylphosphonium iodide
This chemical is primarily used in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the synthesis of pharmaceuticals, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, ensuring selective reactions during multi-step processes. The triphenylphosphonium moiety makes it useful in Wittig reactions, which are employed to form alkenes from carbonyl compounds. This makes it valuable in the production of fine chemicals, agrochemicals, and bioactive compounds. Additionally, its structure allows for modifications in drug discovery, enabling the creation of novel compounds with potential therapeutic applications.
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