trans-4-Amino-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid
95%
- Product Code: 54193
CAS:
369623-85-8
| Molecular Weight: | 230.2609 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07369814 | |
| Melting Point: | Boiling Point: | 371.1 °C at 760 mmHg | |
| Density: | 1.232g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring both an amino group and a carboxylic acid group, makes it a versatile building block for constructing more complex molecules. It is often employed in peptide synthesis, where it serves as a key component for introducing specific functional groups into peptide chains. Additionally, it is used in the preparation of bioactive compounds, including potential drug candidates, due to its ability to enhance stability and bioavailability. The tert-butoxycarbonyl (Boc) protecting group in its structure is particularly valuable in multi-step synthetic processes, as it can be selectively removed under mild conditions without affecting other functional groups. This chemical is also explored in the development of enzyme inhibitors and receptor modulators, contributing to advancements in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿7,920.00 |
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trans-4-Amino-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring both an amino group and a carboxylic acid group, makes it a versatile building block for constructing more complex molecules. It is often employed in peptide synthesis, where it serves as a key component for introducing specific functional groups into peptide chains. Additionally, it is used in the preparation of bioactive compounds, including potential drug candidates, due to its ability to enhance stability and bioavailability. The tert-butoxycarbonyl (Boc) protecting group in its structure is particularly valuable in multi-step synthetic processes, as it can be selectively removed under mild conditions without affecting other functional groups. This chemical is also explored in the development of enzyme inhibitors and receptor modulators, contributing to advancements in medicinal chemistry.
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