tert-Butyl 3-(bromomethyl)-3-methylazetidine-1-carboxylate
≥98%
- Product Code: 65084
CAS:
1408075-52-4
Molecular Weight: | 264.16 g./mol | Molecular Formula: | C₁₀H₁₈BrNO₂ |
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EC Number: | MDL Number: | MFCD23106024 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecules. Its structure, featuring a bromomethyl group and a protected amine, makes it valuable for introducing azetidine rings into target molecules, which are important in medicinal chemistry due to their bioactive properties. It is often employed in the development of pharmaceuticals, particularly in the synthesis of drug candidates that require azetidine moieties for enhanced biological activity. Additionally, the tert-butyl ester group provides stability during reactions, allowing for selective deprotection when needed. This chemical is also useful in cross-coupling reactions and as an intermediate in the preparation of ligands for catalysis.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,031.00 |
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0.250 | 10-20 days | ฿8,541.00 |
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1.000 | 10-20 days | ฿23,040.00 |
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tert-Butyl 3-(bromomethyl)-3-methylazetidine-1-carboxylate
This compound is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecules. Its structure, featuring a bromomethyl group and a protected amine, makes it valuable for introducing azetidine rings into target molecules, which are important in medicinal chemistry due to their bioactive properties. It is often employed in the development of pharmaceuticals, particularly in the synthesis of drug candidates that require azetidine moieties for enhanced biological activity. Additionally, the tert-butyl ester group provides stability during reactions, allowing for selective deprotection when needed. This chemical is also useful in cross-coupling reactions and as an intermediate in the preparation of ligands for catalysis.
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