(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenoxypyrrolidine-2-carboxylic acid
97%
- Product Code: 36581
CAS:
147266-79-3
| Molecular Weight: | 307.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656447 | |
| Melting Point: | Boiling Point: | 455.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex organic molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the presence of the phenoxy group enhances its potential for creating biologically active compounds, such as enzyme inhibitors or receptor modulators, due to its ability to interact with aromatic binding sites in proteins. This chemical is often employed in research and development settings to explore new drug candidates or optimize existing therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,917.00 |
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(2S,4S)-1-(tert-Butoxycarbonyl)-4-phenoxypyrrolidine-2-carboxylic acid
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex organic molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the presence of the phenoxy group enhances its potential for creating biologically active compounds, such as enzyme inhibitors or receptor modulators, due to its ability to interact with aromatic binding sites in proteins. This chemical is often employed in research and development settings to explore new drug candidates or optimize existing therapeutic agents.
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