tert-Butyl 3-(3-hydroxypropyl)azetidine-1-carboxylate
98%
- Product Code: 152849
CAS:
158602-43-8
| Molecular Weight: | 215.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18206284 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure features a protected azetidine ring, which is valuable in medicinal chemistry for enhancing metabolic stability and modulating solubility. The hydroxypropyl side chain allows for further functionalization, enabling conjugation or attachment to other molecular fragments. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting central nervous system disorders and oncology. Its tert-butyl carbamate (Boc) protection group facilitates selective deprotection under mild acidic conditions, making it suitable for multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,080.00 |
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| 0.250 | 10-20 days | ฿3,560.00 |
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| 1.000 | 10-20 days | ฿14,200.00 |
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| 5.000 | 10-20 days | ฿49,500.00 |
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tert-Butyl 3-(3-hydroxypropyl)azetidine-1-carboxylate
Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. Its structure features a protected azetidine ring, which is valuable in medicinal chemistry for enhancing metabolic stability and modulating solubility. The hydroxypropyl side chain allows for further functionalization, enabling conjugation or attachment to other molecular fragments. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting central nervous system disorders and oncology. Its tert-butyl carbamate (Boc) protection group facilitates selective deprotection under mild acidic conditions, making it suitable for multi-step synthetic routes.
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