(2S,4R)-1-((S)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxylic acid
95%
- Product Code: 36548
CAS:
630421-46-4
Molecular Weight: | 344.4000 g./mol | Molecular Formula: | C₁₆H₂₈N₂O₆ |
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EC Number: | MDL Number: | MFCD30729679 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex peptides and pharmaceutical intermediates. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a hydroxyl group, makes it valuable in peptide chemistry for selective deprotection and coupling reactions. It is often employed in the development of protease inhibitors and other bioactive molecules, particularly in medicinal chemistry research. The chiral centers and functional groups allow for precise control in stereoselective synthesis, making it a key building block in the production of targeted therapeutics. Additionally, its stability and reactivity contribute to its use in solid-phase peptide synthesis (SPPS) for constructing peptide chains with high efficiency and purity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿765.00 |
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(2S,4R)-1-((S)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxylic acid
This compound is primarily utilized in the synthesis of complex peptides and pharmaceutical intermediates. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a hydroxyl group, makes it valuable in peptide chemistry for selective deprotection and coupling reactions. It is often employed in the development of protease inhibitors and other bioactive molecules, particularly in medicinal chemistry research. The chiral centers and functional groups allow for precise control in stereoselective synthesis, making it a key building block in the production of targeted therapeutics. Additionally, its stability and reactivity contribute to its use in solid-phase peptide synthesis (SPPS) for constructing peptide chains with high efficiency and purity.
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