tert-Butyl 3-(((methylsulfonyl)oxy)methyl)pyrrolidine-1-carboxylate
≥98%
- Product Code: 59019
CAS:
141699-56-1
| Molecular Weight: | 279.35 g./mol | Molecular Formula: | C₁₁H₂₁NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04038482 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring a pyrrolidine ring and a sulfonate ester group, makes it suitable for various chemical transformations, particularly in the development of pharmaceuticals and bioactive compounds. The tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step syntheses. Additionally, the methylsulfonyloxy (mesylate) group serves as a good leaving group, facilitating nucleophilic substitution reactions to introduce new functional groups. This chemical is often employed in the synthesis of alkaloids, peptidomimetics, and other nitrogen-containing heterocycles, which are essential in drug discovery and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,128.00 |
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| 0.250 | 10-20 days | ฿10,692.00 |
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| 1.000 | 10-20 days | ฿34,092.00 |
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tert-Butyl 3-(((methylsulfonyl)oxy)methyl)pyrrolidine-1-carboxylate
This compound is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its structure, featuring a pyrrolidine ring and a sulfonate ester group, makes it suitable for various chemical transformations, particularly in the development of pharmaceuticals and bioactive compounds. The tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling controlled reactions in multi-step syntheses. Additionally, the methylsulfonyloxy (mesylate) group serves as a good leaving group, facilitating nucleophilic substitution reactions to introduce new functional groups. This chemical is often employed in the synthesis of alkaloids, peptidomimetics, and other nitrogen-containing heterocycles, which are essential in drug discovery and medicinal chemistry.
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