(2S,5S)-1-(tert-Butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid
97%
- Product Code: 36593
CAS:
334769-80-1
| Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13185989 | |
| Melting Point: | Boiling Point: | 343.2±35.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its role as a protected amino acid derivative makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in constructing complex peptide chains with high precision. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during the synthesis process, preventing unwanted side reactions. Additionally, it is employed in the production of chiral intermediates for active pharmaceutical ingredients (APIs), contributing to the creation of enantiomerically pure compounds. Its application extends to research and development in medicinal chemistry, where it aids in exploring new therapeutic agents and optimizing drug efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,782.00 |
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| 1.000 | 10-20 days | ฿4,446.00 |
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| 5.000 | 10-20 days | ฿13,716.00 |
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| 10.000 | 10-20 days | ฿20,592.00 |
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(2S,5S)-1-(tert-Butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs. Its role as a protected amino acid derivative makes it valuable in solid-phase peptide synthesis (SPPS), where it helps in constructing complex peptide chains with high precision. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during the synthesis process, preventing unwanted side reactions. Additionally, it is employed in the production of chiral intermediates for active pharmaceutical ingredients (APIs), contributing to the creation of enantiomerically pure compounds. Its application extends to research and development in medicinal chemistry, where it aids in exploring new therapeutic agents and optimizing drug efficacy.
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