tert-Butyl 3-bromo-3-(hydroxymethyl)azetidine-1-carboxylate
97%
- Product Code: 45188
CAS:
2007919-81-3
| Molecular Weight: | 266.1322 g./mol | Molecular Formula: | C₉H₁₆BrNO₃ |
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| EC Number: | MDL Number: | MFCD29918574 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules, particularly in pharmaceutical research. Its structure, featuring both a bromo and a hydroxymethyl group on the azetidine ring, makes it a valuable building block for constructing nitrogen-containing heterocycles. These heterocycles are often key components in active pharmaceutical ingredients (APIs) and biologically active compounds. The tert-butyl carboxylate group provides stability and facilitates further functionalization through deprotection, enabling chemists to tailor the molecule for specific applications. It is commonly employed in the synthesis of drug candidates targeting neurological disorders, inflammation, and other therapeutic areas. Additionally, its reactive sites allow for the introduction of diverse substituents, making it a useful tool in medicinal chemistry for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,655.00 |
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tert-Butyl 3-bromo-3-(hydroxymethyl)azetidine-1-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules, particularly in pharmaceutical research. Its structure, featuring both a bromo and a hydroxymethyl group on the azetidine ring, makes it a valuable building block for constructing nitrogen-containing heterocycles. These heterocycles are often key components in active pharmaceutical ingredients (APIs) and biologically active compounds. The tert-butyl carboxylate group provides stability and facilitates further functionalization through deprotection, enabling chemists to tailor the molecule for specific applications. It is commonly employed in the synthesis of drug candidates targeting neurological disorders, inflammation, and other therapeutic areas. Additionally, its reactive sites allow for the introduction of diverse substituents, making it a useful tool in medicinal chemistry for structure-activity relationship (SAR) studies.
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