tert-Butyl 3-(2-bromoethyl)azetidine-1-carboxylate
≥95%
- Product Code: 117397
CAS:
1420859-80-8
| Molecular Weight: | 264.16 g./mol | Molecular Formula: | C₁₀H₁₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24382790 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, dry sealed |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the construction of complex organic structures, especially those containing azetidine rings, which are valuable in drug discovery due to their unique pharmacological properties. The bromoethyl group attached to the azetidine ring allows for further functionalization through nucleophilic substitution reactions, enabling the creation of diverse derivatives. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances the stability of the molecule during synthetic processes and can be selectively removed under mild conditions, making it a versatile building block in medicinal chemistry. Its applications are particularly relevant in the synthesis of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,279.00 |
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| 0.250 | 10-20 days | ฿14,112.00 |
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| 1.000 | 10-20 days | ฿37,125.00 |
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tert-Butyl 3-(2-bromoethyl)azetidine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the construction of complex organic structures, especially those containing azetidine rings, which are valuable in drug discovery due to their unique pharmacological properties. The bromoethyl group attached to the azetidine ring allows for further functionalization through nucleophilic substitution reactions, enabling the creation of diverse derivatives. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances the stability of the molecule during synthetic processes and can be selectively removed under mild conditions, making it a versatile building block in medicinal chemistry. Its applications are particularly relevant in the synthesis of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas.
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