(2S,4S)-1-Tert-Butyl 2-Methyl 4-((Tert-Butyldimethylsilyl)Oxy)Pyrrolidine-1,2-Dicarboxylate
98%
- Product Code: 123619
CAS:
367966-45-8
| Molecular Weight: | 359.53 g./mol | Molecular Formula: | C₁₇H₃₃NO₅Si |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 376.8±42.0 °C(Predicted) | |
| Density: | 1.03±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and biologically active molecules. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable in multi-step synthetic processes where selective deprotection is required. It is often employed in the synthesis of complex molecules, such as natural products or drug candidates, where the pyrrolidine ring serves as a key structural motif. The compound's stereochemistry also plays a crucial role in the synthesis of chiral compounds, ensuring the desired enantiomeric purity in the final product. Its application is especially prominent in medicinal chemistry for the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $209.00 |
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| 0.250 | 10-20 days | $348.87 |
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(2S,4S)-1-Tert-Butyl 2-Methyl 4-((Tert-Butyldimethylsilyl)Oxy)Pyrrolidine-1,2-Dicarboxylate
This compound is primarily utilized as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and biologically active molecules. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable in multi-step synthetic processes where selective deprotection is required. It is often employed in the synthesis of complex molecules, such as natural products or drug candidates, where the pyrrolidine ring serves as a key structural motif. The compound's stereochemistry also plays a crucial role in the synthesis of chiral compounds, ensuring the desired enantiomeric purity in the final product. Its application is especially prominent in medicinal chemistry for the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas.
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