N-Boc-3-(aminomethyl)-3-methyloxetane
≥97%
- Product Code: 69596
CAS:
208105-83-3
| Molecular Weight: | 201.26 g./mol | Molecular Formula: | C₁₀H₁₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11656774 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
N-Boc-3-(aminomethyl)-3-methyloxetane is primarily utilized in organic synthesis as a protected intermediate for the preparation of more complex molecules. Its Boc (tert-butoxycarbonyl) group serves as a protective shield for the amine functionality, allowing selective reactions to occur at other sites of the molecule without interference. This compound is particularly valuable in the synthesis of pharmaceuticals, where it can be incorporated into drug candidates to enhance stability or modify biological activity. Additionally, it finds use in the development of agrochemicals and specialty chemicals, where its oxetane ring contributes to unique structural and reactivity properties. After the desired transformations are completed, the Boc group can be easily removed under mild acidic conditions, revealing the free amine for further functionalization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,150.00 |
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| 1.000 | 10-20 days | ฿8,010.00 |
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| 5.000 | 10-20 days | ฿31,500.00 |
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N-Boc-3-(aminomethyl)-3-methyloxetane
N-Boc-3-(aminomethyl)-3-methyloxetane is primarily utilized in organic synthesis as a protected intermediate for the preparation of more complex molecules. Its Boc (tert-butoxycarbonyl) group serves as a protective shield for the amine functionality, allowing selective reactions to occur at other sites of the molecule without interference. This compound is particularly valuable in the synthesis of pharmaceuticals, where it can be incorporated into drug candidates to enhance stability or modify biological activity. Additionally, it finds use in the development of agrochemicals and specialty chemicals, where its oxetane ring contributes to unique structural and reactivity properties. After the desired transformations are completed, the Boc group can be easily removed under mild acidic conditions, revealing the free amine for further functionalization.
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