(2S,4R)-tert-Butyl 4-(((benzyloxy)carbonyl)amino)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
95%
- Product Code: 36556
CAS:
1194057-63-0
| Molecular Weight: | 350.4095 g./mol | Molecular Formula: | C₁₈H₂₆N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18801151 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting neurological and cardiovascular disorders. Its structure, featuring both a hydroxymethyl group and a protected amine, makes it valuable for constructing peptide-like frameworks and other biologically active compounds. Additionally, it is employed in the development of protease inhibitors and other enzyme-targeting drugs, leveraging its ability to mimic natural substrates. The tert-butyl and benzyloxycarbonyl groups provide stability and selective reactivity, facilitating controlled chemical transformations in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,235.00 |
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(2S,4R)-tert-Butyl 4-(((benzyloxy)carbonyl)amino)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting neurological and cardiovascular disorders. Its structure, featuring both a hydroxymethyl group and a protected amine, makes it valuable for constructing peptide-like frameworks and other biologically active compounds. Additionally, it is employed in the development of protease inhibitors and other enzyme-targeting drugs, leveraging its ability to mimic natural substrates. The tert-butyl and benzyloxycarbonyl groups provide stability and selective reactivity, facilitating controlled chemical transformations in multi-step synthetic routes.
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