(2S,4R)-1-((9H-Fluoren-9-yl)methyl) 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
97%(HPLC)
- Product Code: 36960
CAS:
122350-59-8
| Molecular Weight: | 367.40 g./mol | Molecular Formula: | C₂₁H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12545917 | |
| Melting Point: | Boiling Point: | 539°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in peptide chemistry. It serves as a key intermediate in the production of complex peptide structures, where it aids in the protection of functional groups during synthesis. The fluorenylmethyl group acts as a protecting group for amines, ensuring selective reactivity and preventing unwanted side reactions. Its stereochemistry is crucial for the synthesis of enantiomerically pure compounds, making it valuable in the development of pharmaceuticals and bioactive molecules. Additionally, it is employed in the preparation of peptidomimetics and other biologically active compounds, contributing to advancements in drug discovery and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿891.00 |
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| 10.000 | 10-20 days | ฿1,530.00 |
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| 25.000 | 10-20 days | ฿2,754.00 |
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| 100.000 | 10-20 days | ฿8,064.00 |
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(2S,4R)-1-((9H-Fluoren-9-yl)methyl) 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
This compound is primarily utilized in the field of organic synthesis, particularly in peptide chemistry. It serves as a key intermediate in the production of complex peptide structures, where it aids in the protection of functional groups during synthesis. The fluorenylmethyl group acts as a protecting group for amines, ensuring selective reactivity and preventing unwanted side reactions. Its stereochemistry is crucial for the synthesis of enantiomerically pure compounds, making it valuable in the development of pharmaceuticals and bioactive molecules. Additionally, it is employed in the preparation of peptidomimetics and other biologically active compounds, contributing to advancements in drug discovery and medicinal chemistry.
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