(2S, 4S)-methyl 1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidine-2-carboxylate
98%
- Product Code: 70881
CAS:
1318129-60-0
| Molecular Weight: | 349.54 g./mol | Molecular Formula: | C₁₉H₃₁NO₃Si |
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| EC Number: | MDL Number: | MFCD29472562 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a protected hydroxyl group and a carboxylate ester, makes it valuable for constructing chiral pyrrolidine derivatives, which are often found in bioactive compounds and drugs. The tert-butyldimethylsilyl (TBDMS) protecting group ensures selective reactivity during multi-step synthetic processes, allowing chemists to manipulate specific functional groups without interference. Additionally, its chiral centers enable the synthesis of enantiomerically pure compounds, which is crucial in drug development to achieve desired pharmacological effects. This chemical is often employed in the synthesis of antiviral agents, enzyme inhibitors, and other therapeutic molecules targeting various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,200.00 |
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| 0.250 | 10-20 days | ฿11,898.00 |
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| 1.000 | 10-20 days | ฿23,850.00 |
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(2S, 4S)-methyl 1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidine-2-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a protected hydroxyl group and a carboxylate ester, makes it valuable for constructing chiral pyrrolidine derivatives, which are often found in bioactive compounds and drugs. The tert-butyldimethylsilyl (TBDMS) protecting group ensures selective reactivity during multi-step synthetic processes, allowing chemists to manipulate specific functional groups without interference. Additionally, its chiral centers enable the synthesis of enantiomerically pure compounds, which is crucial in drug development to achieve desired pharmacological effects. This chemical is often employed in the synthesis of antiviral agents, enzyme inhibitors, and other therapeutic molecules targeting various diseases.
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