(2R,4S)-2-Hydroxymethyl-4-Boc-aminopyrrolidine hydrochloride
≥95%
- Product Code: 112984
CAS:
1865786-36-2
Molecular Weight: | 252.74 g./mol | Molecular Formula: | C₁₀H₂₁ClN₂O₃ |
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EC Number: | MDL Number: | MFCD11042662 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various therapeutic agents, including antiviral and anticancer drugs. Its chiral structure makes it valuable in creating enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in peptide synthesis, where it acts as a building block for constructing complex peptide chains. Its Boc-protected amino group allows for selective deprotection, enabling precise control over chemical reactions in multi-step synthetic processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿10,017.00 |
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0.250 | 10-20 days | ฿15,426.00 |
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1.000 | 10-20 days | ฿47,403.00 |
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(2R,4S)-2-Hydroxymethyl-4-Boc-aminopyrrolidine hydrochloride
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various therapeutic agents, including antiviral and anticancer drugs. Its chiral structure makes it valuable in creating enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in peptide synthesis, where it acts as a building block for constructing complex peptide chains. Its Boc-protected amino group allows for selective deprotection, enabling precise control over chemical reactions in multi-step synthetic processes.
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