(R)-tert-Butyl 3-formylpyrrolidine-1-carboxylate
98%
- Product Code: 230814
CAS:
191347-94-1
| Molecular Weight: | 199.25 g./mol | Molecular Formula: | C₁₀H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14635728 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its aldehyde functionality allows for versatile transformations such as reductive amination, Wittig reactions, and nucleophilic additions, enabling the construction of complex nitrogen-containing heterocycles. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where the (R)-configuration is critical for biological activity. The tert-butyl carbamate (Boc) group provides stability and acts as a protecting group for the secondary amine, allowing selective reactions at the aldehyde site. Widely utilized in medicinal chemistry and process development for drug discovery programs.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,290.00 |
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| 250mg | 10-20 days | ฿1,850.00 |
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| 1g | 10-20 days | ฿7,380.00 |
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| 5g | 10-20 days | ฿35,000.00 |
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(R)-tert-Butyl 3-formylpyrrolidine-1-carboxylate
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its aldehyde functionality allows for versatile transformations such as reductive amination, Wittig reactions, and nucleophilic additions, enabling the construction of complex nitrogen-containing heterocycles. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where the (R)-configuration is critical for biological activity. The tert-butyl carbamate (Boc) group provides stability and acts as a protecting group for the secondary amine, allowing selective reactions at the aldehyde site. Widely utilized in medicinal chemistry and process development for drug discovery programs.
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