(R)-2-Benzyl 1-tert-butyl 5-oxopyrrolidine-1,2-dicarboxylate
≥95%
- Product Code: 37751
CAS:
400626-71-3
Molecular Weight: | 319.35 g./mol | Molecular Formula: | C₁₇H₂₁NO₅ |
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EC Number: | MDL Number: | MFCD14635665 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both benzyl and tert-butyl ester groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptidomimetics and other bioactive compounds, where the stereochemistry at the chiral center plays a critical role in biological activity. Additionally, its pyrrolidine core is useful in constructing heterocyclic frameworks, which are common in drug discovery. The compound’s stability and reactivity also make it suitable for use in asymmetric synthesis and catalysis studies.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿900.00 |
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0.250 | 10-20 days | ฿1,503.00 |
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1.000 | 10-20 days | ฿4,518.00 |
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(R)-2-Benzyl 1-tert-butyl 5-oxopyrrolidine-1,2-dicarboxylate
This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both benzyl and tert-butyl ester groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptidomimetics and other bioactive compounds, where the stereochemistry at the chiral center plays a critical role in biological activity. Additionally, its pyrrolidine core is useful in constructing heterocyclic frameworks, which are common in drug discovery. The compound’s stability and reactivity also make it suitable for use in asymmetric synthesis and catalysis studies.
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